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安全信息

SAB4501401

Sigma-Aldrich

Anti-HMGB1 antibody produced in rabbit

affinity isolated antibody

别名:

HMG-1, HMG1, High mobility group protein 1, High mobility group protein B1

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About This Item

MDL编号:
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 24 kDa

种属反应性

rat, human, mouse

浓度

~1 mg/mL

技术

ELISA: 1:20000
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 ... HMGB1(3146)

一般描述

Anti-HMGB1 Antibody detects endogenous levels of total HMGB1 protein.
High mobility group box 1 (HMGB1) is a nuclear protein that belongs to the damage-associated molecular pattern (DAMP) family. It is located on human chromosome 13q12.

免疫原

The antiserum was produced against synthesized peptide derived from human HMGB1.

Immunogen Range: 131-180

生化/生理作用

High mobility group box 1 (HMGB1) is involved in bone remodeling and ectopic calcification pathogenesis. It initiates neuroinflammation after epileptogenic injuries. HMGB1 also binds to chromatin and modulates gene transcription.

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.

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WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Roles of High Mobility Group Box 1 in Cardiovascular Calcification.
Chen Q, et al.
Cellular Physiology and Biochemistry, 42(2), 427-440 (2017)
A new case of 13q12.2q13.1 microdeletion syndrome contributes to phenotype delineation.
Mandrile G,et al.
Case Reports in Genetics (2014)
Molecular isoforms of high-mobility group box 1 are mechanistic biomarkers for epilepsy.
Walker LE, et al.
The Journal of Clinical Investigation, 127(6), 2118-2132 (2017)
Laura Patricia Whittall-Garcia et al.
Lupus science & medicine, 11(1) (2024-01-05)
To determine if the serum levels of neutrophil extracellular trap (NET) remnants (Elastase-DNA and HMGB1-DNA complexes) at the time of a lupus nephritis (LN) flare predict renal outcomes in the following 24 months. This was a retrospective study performed in

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