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ADAMTS13 (基因名), A disintegrin and metalloproteinase with thrombospondin motifs 13 (蛋白名), ats13_human.
产品名称:

Human ADAMTS13/ A disintegrin and metalloproteinase with thrombospondin motifs 13 Recombinant Protein
去整合素金属蛋白酶含血小板反应蛋白13

货号:

R0950h

商标:
EIAab®
监管等级:
别名:

von Willebrand factor-cleaving protease, vWF-CP, UNQ6102/PRO20085, ADAM-TS 13, C9orf8

序列号:
Q76LX8
来源:
E.coli
种属:
Human
标签:
His
序列:
391-565aa
预估分子量:
19.25 kDa (monomer)
纯度:
Greater than 90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human ADAMTS13 Protein
规格 & 价格: cart
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Human ADAMTS13 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
Human ADAMTS13 Protein
Recombinant human ADAMTS13 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 9q34.2 by HGNC 9q34.2 by Entrez Gene 9q34.2 by Ensembl
ADAMTS13 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
N/A


功能:
Cleaves the vWF multimers in plasma into smaller forms thereby controlling vWF-mediated platelet thrombus formation.


亚细胞位置:
Secreted Secretion enhanced by O-fucosylation of TSP type-1 repeats.


该产品尚未在任何出版物中被引用。

[1].
"ADAMTS13 mutations and polymorphisms in congenital thrombotic thrombocytopenic purpura."

[2].
"Lower levels of ADAMTS13 are associated with cardiovascular disease in young patients."

[3].
"Frequency of Pro475Ser polymorphism of ADAMTS13 gene and its association with ADAMTS-13 activity in the Korean population."

[4].
"Prevalence of the ADAMTS-13 missense mutation R1060W in late onset adult thrombotic thrombocytopenic purpura."

[5].
"O-fucosylation is required for ADAMTS13 secretion."

[6].
"Zinc and calcium ions cooperatively modulate ADAMTS13 activity."

[7].
"Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome)."

[8].
"Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13."

[9].
"ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13."

[10].
"Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity."
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