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多克隆抗體

CHST6 rabbit Polyclonal Antibody

CHST6抗體
CHST6抗體應(yīng)用:Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000. carbohydrate sulfotransferase 6(CHST6) Homo sapiens The protein encoded by this gene is an enzyme that catalyzes the transfer of a sulfate group to the GlcNAc residues of keratan. Keratan sulfate helps maintain corneal transparency. Defects in this gene are a cause of macular corneal dystrophy (MCD). [provided by RefSeq, Jan 2010],

CHST9 rabbit Polyclonal Antibody

CHST9抗體
CHST9抗體應(yīng)用:Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000.carbohydrate sulfotransferase 9(CHST9) Homo sapiens The protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of non-reducing N-acetylgalactosamine (GalNAc) residues in both N-glycans and O-glycans. Sulfate groups on carbohydrates confer highly specific functions to glycoproteins, glycolipids, and proteoglycans, and are critical for cell-cell interaction, signal transduction, and embryonic development. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Aug 2011],

CHSY1 rabbit Polyclonal Antibody

CHSY1抗體
CHSY1抗體應(yīng)用:Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. chondroitin sulfate synthase 1(CHSY1) Homo sapiens This gene encodes a member of the chondroitin N-acetylgalactosaminyltransferase family. These enzymes possess dual glucuronyltransferase and galactosaminyltransferase activity and play critical roles in the biosynthesis of chondroitin sulfate, a glycosaminoglycan involved in many biological processes including cell proliferation and morphogenesis. Decreased expression of this gene may play a role in colorectal cancer, and mutations in this gene are a cause of temtamy preaxial brachydactyly syndrome. [provided by RefSeq, Dec 2011],

CHSY2 rabbit Polyclonal Antibody

CHSY2抗體
CHSY2抗體應(yīng)用:WB 1:500-2000 catalytic activity:UDP-alpha-D-glucuronate + N-acetyl-beta-D-galactosaminyl-(1->4)-beta-D-glucuronosyl-proteoglycan = UDP + beta-D-glucuronosyl-(1->3)-N-acetyl-beta-D-galactosaminyl-(1->4)-beta-D-glucuronosyl-proteoglycan.,catalytic activity:UDP-N-acetyl-D-galactosamine + beta-D-glucuronosyl-(1->3)-N-acetyl-beta-D-galactosaminyl-proteoglycan = UDP + N-acetyl-beta-D-galactosaminyl-(1->4)-beta-D-glucuronosyl-(1->3)-N-acetyl-beta-D-galactosaminyl-proteoglycan.,cofactor:Divalent cations. Highest activities are measured with manganese. Can also utilize cobalt.,function:Has both beta-1,3-glucuronic acid and beta-1,4-N-acetylgalactosamine transferase activity. Transfers glucuronic acid (GlcUA) from UDP-GlcUA and N-acetylgalactosamine (GalNAc) from UDP-GalNAc to the non-reducing end of the elongating chondroitin polymer.,online information:GlycoGene database,PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Belongs to the chondroitin N-acetylgalacto

Chymase rabbit Polyclonal Antibody

Chymase抗體
Chymase抗體應(yīng)用:Western Blot: 1/500 - 1/2000. ELISA: 1/20000. chymase 1(CMA1) Homo sapiens This gene encodes a chymotryptic serine proteinase that belongs to the peptidase family S1. It is expressed in mast cells and is thought to function in the degradation of the extracellular matrix, the regulation of submucosal gland secretion, and the generation of vasoactive peptides. In the heart and blood vessels, this protein, rather than angiotensin converting enzyme, is largely responsible for converting angiotensin I to the vasoactive peptide angiotensin II. Alternative splicing results in multiple variants. [provided by RefSeq, Apr 2015],

CI092 rabbit Polyclonal Antibody

CI092抗體
CI092抗體應(yīng)用:IHC-p 1:50-200

CI123 rabbit Polyclonal Antibody

CI123抗體
CI123抗體應(yīng)用:WB 1:500-2000

CI153 rabbit Polyclonal Antibody

CI153抗體
CI153抗體應(yīng)用:IHC-p 1:50-200

CIB2 rabbit Polyclonal Antibody

CIB2抗體
CIB2抗體應(yīng)用:Immunohistochemistry: 1/100 - 1/300. ELISA: 1/5000. calcium and integrin binding family member 2(CIB2) Homo sapiens The protein encoded by this gene is similar to that of KIP/CIB, calcineurin B, and calmodulin. The encoded protein is a calcium-binding regulatory protein that interacts with DNA-dependent protein kinase catalytic subunits (DNA-PKcs), and it is involved in photoreceptor cell maintenance. Mutations in this gene cause deafness, autosomal recessive, 48 (DFNB48), and also Usher syndrome 1J (USH1J). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014],

CIB3 rabbit Polyclonal Antibody

CIB3抗體
CIB3抗體應(yīng)用:Western Blot: 1/500 - 1/2000. ELISA: 1/20000. calcium and integrin binding family member 3(CIB3) Homo sapiens This gene product shares a high degree of sequence similarity with DNA-dependent protein kinase catalytic subunit-interacting protein 2 in human and mouse, and like them may bind the catalytic subunit of DNA-dependent protein kinases. The exact function of this gene is not known. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014],
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