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安全信息

SAB4500827

Sigma-Aldrich

Anti-Factor VIII antibody produced in rabbit

affinity isolated antibody

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别名:
AHF, F8B, F8C, antihemophilic factor, coagulation factor VIII
UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

rabbit

质量水平

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

形式

buffered aqueous solution

分子量

antigen 267 kDa

种属反应性

mouse, human

浓度

~1 mg/mL

技术

ELISA: 1:10000
western blot: 1:500-1:1000

NCBI登记号

UniProt登记号

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... F8(2157)

一般描述

Anti-Factor VIII Antibody detects endogenous levels of total Factor VIII protein.
Blood clotting factor VIII (FVIII), a nonenzymatic cofactor of activated factor IX (FIXa) is of ~330 kDa. It has three homologous A-domains, a unique B-domain and two C-domains. It is located on chromosome Xq28.

免疫原

The antiserum was produced against synthesized peptide derived from human Factor VIII.

Immunogen Range: 2161-2210

生化/生理作用

Mutation in the factor VIII gene (F8) results in haemophilia A (HA). Higher levels of VIII:C (FVIII:C) leads to venous and arterial thromboembolism. The factor VIII serve as a procoagulant cofactor in the intrinsic blood coagulation pathway.

特点和优势

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

外形

Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品

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Mutational spectrum and deep intronic variants in the factor VIII gene of haemophilia A patients. Identification by next generation sequencing
Bach JE, et al.
Hamostaseologie, 36(S 02), S25-S28 (2016)
Localization of human factor FVIII inhibitor epitopes to two polypeptide fragments
Fulcher CA, et al.
Proceedings of the National Academy of Sciences of the USA, 82(22), 7728-7732 (1985)
Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28
Kyndt F, et al.
American Journal of Human Genetics, 62(3), 627-632 (1998)
Elevated levels of FVIII:C within families are associated with an increased risk for venous and arterial thrombosis
Bank I, et al.
Journal of Thrombosis and Haemostasis, 3(1), 79-84 (2005)
An in silico and in vitro approach to elucidate the impact of residues flanking the cleavage scissile bonds of FVIII
Pezeshkpoor B, et al.
PLoS ONE, 12(7) (2017)

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