Paracrine elements of mesenchymal stem cells recruit macrophages and endothelial lineage cells and improve wound therapeutic.
Bone marrow derived mesenchymal stem cells (BM-MSCs) have been proven to reinforce wound therapeutic; nevertheless, the mechanisms concerned are barely understood.
On this examine, we examined paracrine elements launched by BM-MSCs and their results on the cells taking part in wound therapeutic in comparison with these launched by dermal fibroblasts.
Analyses of BM-MSCs with Actual-Time PCR and of BM-MSC-conditioned medium by antibody-based protein array and ELISA indicated that BM-MSCs secreted distinctively completely different cytokines and chemokines, similar to higher quantities of VEGF-alpha, IGF-1, EGF, keratinocyte progress issue, angiopoietin-1, stromal derived factor-1, macrophage inflammatory protein-1alpha and beta and erythropoietin, in comparison with dermal fibroblasts.
These molecules are identified to be vital in regular wound therapeutic. BM-MSC-conditioned medium considerably enhanced migration of macrophages, keratinocytes and endothelial cells and proliferation of keratinocytes and endothelial cells in comparison with fibroblast-conditioned medium.
Furthermore, in a mouse mannequin of excisional wound therapeutic, the place concentrated BM-MSC-conditioned medium was utilized, accelerated wound therapeutic occurred in comparison with administration of pre-conditioned or fibroblast-conditioned medium.
Evaluation of cell suspensions derived from the wound by FACS confirmed that wounds handled with BM-MSC-conditioned medium had elevated proportions of CD4/80-positive macrophages and Flk-1-, CD34- or c-package-positive endothelial (progenitor) cells in comparison with wounds handled with pre-conditioned medium or fibroblast-conditioned medium.
Constant with the above findings, immunohistochemical evaluation of wound sections confirmed that wounds handled with BM-MSC-conditioned medium had elevated abundance of macrophages.
Our outcomes recommend that elements launched by BM-MSCs recruit macrophages and endothelial lineage cells into the wound thus enhancing wound therapeutic.
Description: Description of target: Transcriptional coactivator for steroid receptors and nuclear receptors. Greatly increases the transcriptional activity of PPARG and thyroid hormone receptor on the uncoupling protein promoter. Can regulate key mitochondrial genes that contribute to the program of adaptive thermogenesis. Plays an essential role in metabolic reprogramming in response to dietary availability through coordination of the expression of a wide array of genes involved in glucose and fatty acid metabolism. Induces the expression of PERM1 in the skeletal muscle in an ESRRA-dependent manner. Also involved in the integration of the circadian rhythms and energy metabolism. Required for oscillatory expression of clock genes, such as ARNTL/BMAL1 and NR1D1, through the coactivation of RORA and RORC, and metabolic genes, such as PDK4 and PEPCK. ;Species reactivity: Rat;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.078 ng/mL
Description: Description of target: Transcriptional coactivator for steroid receptors and nuclear receptors. Greatly increases the transcriptional activity of PPARG and thyroid hormone receptor on the uncoupling protein promoter. Can regulate key mitochondrial genes that contribute to the program of adaptive thermogenesis. Plays an essential role in metabolic reprogramming in response to dietary availability through coordination of the expression of a wide array of genes involved in glucose and fatty acid metabolism. Induces the expression of PERM1 in the skeletal muscle in an ESRRA-dependent manner. Also involved in the integration of the circadian rhythms and energy metabolism. Required for oscillatory expression of clock genes, such as ARNTL/BMAL1 and NR1D1, through the coactivation of RORA and RORC, and metabolic genes, such as PDK4 and PEPCK.;Species reactivity: Pig;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.048 ng/mL
Description: Description of target: This gene encodes a transcriptional coactivator that induces and coordinates gene expression regulating mitochondrial biogenesis, respiration, hepatic gluconeogenesis, thermogenic program in brown fat and muscle fiber-type switching. Mice lacking the encoded protein exhibit reduced thermogenic capacity, hyperactivity and resistance to diet-induced obesity. Mice lacking the encoded protein specifically in the heart exhibit peripartum cardiomyopathy. Alternative splicing results in multiple transcript variants.;Species reactivity: Mouse;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.055 ng/mL
Description: Description of target: The protein encoded by this gene is a transcriptional coactivator that regulates the genes involved in energy metabolism. This protein interacts with PPARgamma, which permits the interaction of this protein with multiple transcription factors. This protein can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination. This protein may be also involved in controlling blood pressure, regulating cellular cholesterol homoeostasis, and the development of obesity.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.055 ng/mL
Description: Description of target: PPARGC1A is a transcriptional coactivator that regulates the genes involved in energy metabolism. This protein interacts with PPARgamma, which permits the interaction of this protein with multiple transcription factors. This protein can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination. This protein may be also involved in controlling blood pressure, regulating cellular cholesterol homoeostasis, and the development of obesity.The protein encoded by this gene is a transcriptional coactivator that regulates the genes involved in energy metabolism. This protein interacts with PPARgamma, which permits the interaction of this protein with multiple transcription factors. This protein can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination. This protein may be also involved in controlling blood pressure, regulating cellular cholesterol homoeostasis, and the development of obesity. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.055ng/mL
Description: Description of target: Ppargc1a is a transcriptional coactivator for steroid receptors and nuclear receptors. Ppargc1a greatly increases the transcriptional activity of PPARG and thyroid hormone receptor on the uncoupling protein promoter. Ppargc1a can regulate key mitochondrial genes that contribute to the program of adaptive thermogenesis.;Species reactivity: Mouse;Application: ELISA;Assay info: ;Sensitivity: < 0.056ng/mL
Description: Description of target: Transcriptional coactivator for steroid receptors and nuclear receptors. Greatly increases the transcriptional activity of PPARG and thyroid hormone receptor on the uncoupling protein promoter. Can regulate key mitochondrial genes that contribute to the program of adaptive thermogenesis. Plays an essential role in metabolic reprogramming in response to dietary availability through coordination of the expression of a wide array of genes involved in glucose and fatty acid metabolism. Induces the expression of PERM1 in the skeletal muscle in an ESRRA-dependent manner. Also involved in the integration of the circadian rhythms and energy metabolism. Required for oscillatory expression of clock genes, such as ARNTL/BMAL1 and NR1D1, through the coactivation of RORA and RORC, and metabolic genes, such as PDK4 and PEPCK. Isoform 4 specifically activates the expression of IGF1 and suppresses myostatin expression in skeletal muscle leading to muscle fiber hypertrophy.4 Publications;Species reactivity: Mouse;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.078 ng/mL
Description: Description of target: Transcriptional coactivator for steroid receptors and nuclear receptors. Greatly increases the transcriptional activity of PPARG and thyroid hormone receptor on the uncoupling protein promoter. Can regulate key mitochondrial genes that contribute to the program of adaptive thermogenesis. Plays an essential role in metabolic reprogramming in response to dietary availability through coordination of the expression of a wide array of genes involved in glucose and fatty acid metabolism. Induces the expression of PERM1 in the skeletal muscle in an ESRRA-dependent manner. Also involved in the integration of the circadian rhythms and energy metabolism. Required for oscillatory expression of clock genes, such as ARNTL/BMAL1 and NR1D1, through the coactivation of RORA and RORC, and metabolic genes, such as PDK4 and PEPCK.;Species reactivity: Bovine;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.097 ng/mL
Description: Description of target: Transcriptional coactivator for steroid receptors and nuclear receptors. Greatly increases the transcriptional activity of PPARG and thyroid hormone receptor on the uncoupling protein promoter. Can regulate key mitochondrial genes that contribute to the program of adaptive thermogenesis. Plays an essential role in metabolic reprogramming in response to dietary availability through coordination of the expression of a wide array of genes involved in glucose and fatty acid metabolism. Induces the expression of PERM1 in the skeletal muscle in an ESRRA-dependent manner. Also involved in the integration of the circadian rhythms and energy metabolism. Required for oscillatory expression of clock genes, such as ARNTL/BMAL1 and NR1D1, through the coactivation of RORA and RORC, and metabolic genes, such as PDK4 and PEPCK. ;Species reactivity: Human;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.19 ng/mL
Description: The peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PPARGC1A), also known as LEM-6, is a transcriptional coactivator that regulates the genes involved in energy metabolism (1). PPARGC1A interacts with PPARgamma, which permits the interaction of PPARGC1A with multiple transcription factors. PPARGC1A can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination (2). PPARGC1A may be also involved in the development of obesity (3).
Description: The peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PPARGC1A), also known as LEM-6, is a transcriptional coactivator that regulates the genes involved in energy metabolism (1). PPARGC1A interacts with PPARgamma, which permits the interaction of PPARGC1A with multiple transcription factors. PPARGC1A can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination (2). PPARGC1A may be also involved in the development of obesity (3).
Description: The peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PPARGC1A), also known as LEM-6, is a transcriptional coactivator that regulates the genes involved in energy metabolism (1). PPARGC1A interacts with PPARgamma, which permits the interaction of PPARGC1A with multiple transcription factors. PPARGC1A can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination (2). PPARGC1A may be also involved in the development of obesity (3).
Description: The peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PPARGC1A), also known as LEM-6, is a transcriptional coactivator that regulates the genes involved in energy metabolism (1). PPARGC1A interacts with PPARgamma, which permits the interaction of PPARGC1A with multiple transcription factors. PPARGC1A can interact with, and regulate the activities of, cAMP response element binding protein (CREB) and nuclear respiratory factors (NRFs). It provides a direct link between external physiological stimuli and the regulation of mitochondrial biogenesis, and is a major factor that regulates muscle fiber type determination (2). PPARGC1A may be also involved in the development of obesity (3).
Description: A polyclonal antibody against PPARGC1A. Recognizes PPARGC1A from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB;ELISA:1:1000-1:2000, WB:1:200-1:1000
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human PPARGC1A . This antibody is tested and proven to work in the following applications:
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human PPARGC1A . This antibody is tested and proven to work in the following applications:
Description: A sandwich quantitative ELISA assay kit for detection of Rat Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in samples from tissue homogenates, cell lysates or other biological fluids.
Description: A sandwich quantitative ELISA assay kit for detection of Rat Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in samples from tissue homogenates, cell lysates or other biological fluids.
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in tissue homogenates, cell lysates and other biological fluids.
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in tissue homogenates, cell lysates and other biological fluids.
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in tissue homogenates, cell lysates and other biological fluids.
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in tissue homogenates, cell lysates and other biological fluids.
Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Rat Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in samples from tissue homogenates, cell lysates and other biological fluids with no significant corss-reactivity with analogues from other species.
Description: Quantitativesandwich ELISA kit for measuring Rat Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PPARGC1A) in samples from serum, plasma, cell culture supernates, cell lysates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Rat Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PPARGC1A) ELISA kit
Description: Quantitativesandwich ELISA kit for measuring Rat Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PPARGC1A) in samples from serum, plasma, cell culture supernates, cell lysates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: A sandwich ELISA kit for detection of Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha from Rat in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
Description: A sandwich quantitative ELISA assay kit for detection of Human Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in samples from tissue homogenates, cell lysates or other biological fluids.
Description: A sandwich quantitative ELISA assay kit for detection of Human Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in samples from tissue homogenates, cell lysates or other biological fluids.
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Peroxisome Proliferator Activated Receptor Gamma Coactivator 1 Alpha (PPARgC1a) in samples from tissue homogenates, cell lysates or other biological fluids.
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Anopheles funestus immune to pyrethroid pesticides in South Africa.
Northern Kwazulu/Natal (KZN) Province of South Africa borders on southern Mozambique, between Swaziland and the Indian Ocean.
To management malaria vectors in KZN, homes had been sprayed yearly with residual DDT 2 g/ m2 till 1996 when the remedy modified to deltamethrin 20-25 mg/m2.
At Ndumu (27 levels 02’S, 32 levels 19’E) the recorded malaria incidence elevated greater than six-fold between 1995 and 1999.
Entomological surveys throughout late 1999 discovered mosquitoes of the Anopheles funestus group (Diptera: Culicidae) resting in sprayed homes in some sectors of Ndumu space.
This very endophilic-vector of malaria had been eradicated from South Africa by DDT spraying within the 1950s, leaving the much less endophilic .
An arabiensis Patton as the one vector of identified significance in KZN. Deltamethrin-sprayed homes at Ndumu had been checked for insecticide efficacy by bioassay utilizing vulnerable An. arabiensis (laboratory-reared) that demonstrated 100% mortality.
Members of the An. funestus group from Ndumu homes (29 males, 116 females) had been recognized by the rDNA PCR technique and 4 species had been discovered: 74 .
An funestus Giles sensu stricto, 34 An. parensis Gillies, seven. An rivulorum Leeson and one An. leesoni Evans. Amongst An. funestus s.s. females, 5.4% (4/74) had been constructive for Plasmodium falciparum by ELISA and PCR checks.
To check for pyrethroid resistance, mosquito adults had been uncovered to permethrin discriminating dosage and mortality scored 24h post-exposure: survival charges of wild-caught wholesome males had been 5/10 An. funestus, 1/9 An. rivulorum and 0/2 An. parensis; survival charges of laboratory-reared grownup progeny from 19 An. funestus females averaged 14% (after 1h publicity to 1% permethrin 25:75cis:trans on papers in WHO check kits) and 27% (after 30 min in a bottle with 25 microg permethrin 40:60cis:trans).
Anopheles funestus households displaying >20% survival in these two resistance check procedures numbered 5/19 and 12/19, respectively. Progeny from 15 of the households had been examined on 4% DDT impregnated papers and gave 100% mortality.
Discovering these proportions of pyrethroid-resistant An. funestus, related with a malaria upsurge at Ndumu, has severe implications for malaria vector management operations in southern Africa.
Professional- and anti inflammatory types of interleukin-1 within the tear fluid and conjunctiva of sufferers with dry-eye illness.
OBJECTIVE
To examine the expression of the pro- and anti inflammatory types of interleukin (IL)-1 within the tear fluid and conjunctival epithelium of regular eyes and people with dry-eye illness.
METHODS
The concentrations of IL-1 alpha, IL-1 beta (precursor and mature varieties), and IL-1 receptor antagonist (IL-1Ra) had been measured by ELISA in tear fluid samples obtained from regular people and sufferers with dry eye who had rosacea-associated meibomian gland illness (MGD) or Sjögren’s syndrome (SS) aqueous tear deficiency (ATD).
These cytokines had been additionally measured in regular tear fluid earlier than and after nasal stimulation to induce reflex tearing. The relative expression of those cytokines was evaluated in conjunctival impression cytology specimens and conjunctival biopsy tissue obtained from regular topics and SS ATD-affected sufferers utilizing immunofluorescent staining.
Matrix metalloproteinase (MMP)-9 focus and exercise within the tear fluid had been evaluated with gelatin zymography and with an MMP-9 exercise assay package, respectively.
RESULTS
In contrast with regular topics, the focus of IL-1 alpha and mature IL-1 beta within the tear fluid was elevated, and the focus of precursor IL-1 beta was decreased in sufferers with MGD (P < 0.05, P = 0.02, and P < 0.01, respectively) and SS ATD (P < 0.001, P = 0.02, and P < 0.001, respectively).
There was no important change within the focus of IL-1 alpha, precursor IL-1 beta, and IL-1Ra in reflex tear fluid, indicating that the lacrimal glands could secrete these cytokines. The exercise of MMP-9, a physiological activator of IL-1 beta, was considerably elevated within the tear fluid of each dry-eye teams in contrast with regular topics.
A robust constructive correlation was noticed between the depth of corneal fluorescein staining and the tear fluid IL-1 alpha focus (r(2) = 0.17, P < 0.02) and the mature-to-precursor IL-1 beta ratio (r(2) = 0.46, P < 0.001).
Optimistic immunofluorescent staining for IL-1 alpha, mature IL-1 beta, and IL-1Ra was noticed in a considerably higher proportion of conjunctival cytology specimens from eyes with SS ATD than in these from regular eyes (P < 0.01 for IL-1 alpha, P < 0.009 for mature IL-1 beta, and P < 0.05 for IL-1Ra).
CONCLUSIONS
Dry-eye illness is accompanied by a rise within the proinflammatory types of IL-1 (IL-1 alpha and mature IL-1 beta) and a lower within the biologically inactive precursor IL-1 beta in tear fluid.
Elevated protease exercise on the ocular floor could also be one mechanism by which precursor IL-1 beta is cleaved to the mature, biologically lively type.
The conjunctival epithelium seems to be one supply of the elevated focus of IL-1 within the tear fluid of sufferers with dry-eye illness.
These resultssuggest that IL-1 could play a key position within the pathogenesis of keratoconjunctivitis sicca.
Description: A rapid test for detection of antibodies (IgG and IgM) for 2019-nCoV, the novel Coronavirus from the Wuhan strain. The test is easy to perform, takes 10 minutes to provide reliable results and is higly specific to the 2019-nCoV Coronavirus.
Description: Human Anti-2019 nCoV(N) IgG ELISA Kitis immunoassay kit allows for the qualitative determination of nCoV-IgG antibody in human serum, plasma, saliva and nasal fluid
Description: Monkeypox virus is the virus that causes the disease monkeypox in both humans and animals. Monkeypox virus is an Orthopoxvirus, a genus of the family Poxviridae that contains other viral species that target mammals. The virus is mainly found in tropical rainforest regions of central and West Africa. The primary route of infection is thought to be contact with the infected animals or their bodily fluids. The genome is not segmented and contains a single molecule of linear double-stranded DNA, 185000 nucleotides long. The Monkeypox Virus real time PCR Kit contains a specific ready-to-use system for the detection of the Monkeypox Virusthrough polymerase chain reaction (PCR) in the real-time PCR system. The master contains reagents and enzymes for the specific amplification of the Monkeypox Virus DNA. Fluorescence is emitted and measured by the real time systems ́ optical unit during the PCR. The detection of amplified Monkeypox Virus DNA fragment is performed in fluorimeter channel 530nm with the fluorescent quencher BHQ1. DNA extraction buffer is available in the kit and serum or lesion exudate samples are used for the extraction of the DNA. In addition, the kit contains a system to identify possible PCR inhibition by measuring the 560nm fluorescence of the internal control (IC). An external positive control defined as 1×10^7 copies/ml is supplied which allow the determination of the gene load.
Description: Monkeypox virus is the virus that causes the disease monkeypox in both humans and animals. Monkeypox virus is an Orthopoxvirus, a genus of the family Poxviridae that contains other viral species that target mammals. The virus is mainly found in tropical rainforest regions of central and West Africa. The primary route of infection is thought to be contact with the infected animals or their bodily fluids.The genome is not segmented and contains a single molecule of linear double-stranded DNA, 185000 nucleotides long.The Monkeypox Virus real time PCR Kit contains a specific ready-to-use system for the detection of the Monkeypox Virusthrough polymerase chain reaction (PCR) in the real-time PCR system. The master contains reagents and enzymes for the specific amplification of theMonkeypox VirusDNA. Fluorescence is emitted and measured by the real time systems ́ optical unit during the PCR. The detection of amplified Monkeypox Virus DNA fragment is performed in fluorimeter channelFAM with the fluorescent quencher BHQ1. DNA extraction buffer is available in the kit and serum or lesion exudate samples are used for the extraction of the DNA. In addition, the kit contains a system to identify possible PCR inhibition by measuring the HEX/VIC/JOE fluorescence of the internal control (IC). An external positive control defined as 1×107copies/ml is supplied which allow the determination of the gene load.
Description: Recombinant Human IL-4 produced in E.Coli is a single, non-glycosylated polypeptide chain containing 130 amino acids and having a molecular mass of 15000 Dalton. The rHuIL-4 is purified by proprietary chromatographic techniques.
SDS-Blue™ - Coomassie based solution for protein staining in SDS-PAGE
Description: SDS-Blue™ is an innovative patented formula, based on Coomassie blue, that comes in a convenient ready to use format for staining proteins in SDS-PAGE (sodium dodecyl sulphate–polyacrylamide gel electrophoresis). The formulation of SDS-Blue™ provides numerous advantages compared to the classic Coomassie staining or to other similar protein stains. SDS-Blue™ provides higher sensitivity, virtually no background and eliminates the need for destaining of the gel due to its high specificity and affinity to bind to protein only. Not only does SDS-Blue™ yield clear and sharp bands, but it also contains no methanol and acetic acid, making it non-hazardous, safe to handle and friendly to the environment when disposed of. Two other advantages that make SDS-Blue™ the better option is that it is not light sensitive and can be stored at ambient temperature for 24 months. And this provides a considerable convenience, especially to laboratories that need and keep big amount of protein staining solutions – no more jammed refrigerators, you can keep SDS-Blue™ wherever it is most convenient for You!
Description: Recombinant human interleukin-2 is a sterile protein product for injection. rHuIL-2 is produced by recombinant DNA technology using Yeast. It is a highly purified protein containing 133 amino acids, with cysteine mutated to alanine at 125 amino acid position, and has a molecular weight of approximately 15.4kD, non-glycosylated.
Description: Recombinant human interleukin-2 is a sterile protein product for injection. rHuIL-2 is produced by recombinant DNA technology using Yeast. It is a highly purified protein containing 133 amino acids, with cysteine mutated to alanine at 125 amino acid position, and has a molecular weight of approximately 15.4kD, non-glycosylated.
Description: Recombinant human GM-CSF produced in E.coli is a single, non-glycosylated, polypeptide chain containing 127 amino acids, two pairs of disulfide bonds and having a molecular mass of approximately 14.5kD.
Andres
