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F13B (基因名), Coagulation factor XIII B chain (蛋白名), f13b_human.
产品名称:

Human F13B/ Coagulation factor XIII B chain Recombinant Protein
HumanCoagulationfactorXIIIBchain

货号:

R15162h

商标:
EIAab®
监管等级:
别名:

Fibrin-stabilizing factor B subunit, Protein-glutamine gamma-glutamyltransferase B chain, Transglutaminase B chain

序列号:
P05160
来源:
E.coli
种属:
Human
标签:
His
序列:
416-661aa
预估分子量:
27.06 kDa (monomer)
纯度:
Greater than 95% 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 F13B Protein
规格 & 价格: cart
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Human F13B 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 F13B Protein
Recombinant human F13B protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 1q31.3 by HGNC 1q31.3 by Entrez Gene 1q31.3 by Ensembl
F13B 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:
Tetramer of two A chains (F13A1) and two B (F13B) chains.


功能:
The B chain of factor XIII is not catalytically active, but is thought to stabilize the A subunits and regulate the rate of transglutaminase formation by thrombin.


亚细胞位置:
Secreted


该产品尚未在任何出版物中被引用。

[1].
"A novel polymorphism in the factor XIII B-subunit (His95Arg): relationship to subunit dissociation and venous thrombosis."

[2].
"Nucleotide sequence of the gene for the b subunit of human factor XIII."

[3].
"Complete cDNA sequence encoding the B subunit of human factor XIII."

[4].
"Genes influencing coagulation and the risk of aneurysmal subarachnoid hemorrhage, and subsequent complications of secondary cerebral ischemia and rebleeding."

[5].
"Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect."

[6].
"A highly sensitive chemiluminescence immunoassay for the measurement of coagulation factor XIII subunits and their complex in tears."

[7].
"Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes."

[8].
"Dengue hemorrhagic fever is associated with polymorphisms in JAK1."

[9].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[10].
"A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM)."
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