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Merck
CN

MABN92-AF488

Sigma-Aldrich

Anti-Iba1/AIF1 Antibody, clone 20A12.1, Alexa Fluor 488 Conjugate

clone 20A12.1, from mouse, ALEXA FLUOR 488

别名:

Allograft inflammatory factor 1, AIF-1, Daintain, Interferon gamma responsive transcript, Ionized calcium-binding adapter molecule 1, Protein G1

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关于此项目

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.45
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生物来源

mouse

质量水平

偶联物

ALEXA FLUOR 488

抗体形式

purified antibody

抗体产品类型

primary antibodies

克隆

20A12.1, monoclonal

种属反应性

human, mouse, rat

技术

immunohistochemistry: suitable

同位素/亚型

IgG1κ

NCBI登记号

UniProt登记号

运输

wet ice

靶向翻译后修饰

unmodified

基因信息

human ... AIF1(199)

一般描述

Allograft inflammatory factor 1 (UniProt P55008; also known as AIF-1, Daintain, Interferon gamma responsive transcript, Ionized calcium-binding adapter molecule 1, Protein G1) is encoded by the AIF1 (also known as G1, IBA1) gene (Gene ID 199) in human. Iba1/AIF1 is a 17 kDa interferon-gamma- (IFN-gamma-) inducible, Ca(2+)-binding EF-hand protein. Iba1/AIF1 expression is mostly limited to the macrophage/monocyte lineage, and is augmented by cytokines, such as IFN-gamma. It is reported to be involved in neuronal function, inflammatory responses, allograft rejection, autoimmunity, and macrophage activation/function. It is also shown to be expressed in microglial cells in autominnume disesase models such as experimental autoimmune encephalomyelitis, neuritis and uveitis.
~17 kDa observed

应用

Anti-Iba1/AIF1 Antibody, clone 20A12.1, Alexa Fluor 488 Conjugate is an antibody against Iba1/AIF1 for use in Immunohistochemistry.

分析说明

Evaluated by Immunohistochemistry in human spleen tissue.

Immunohistochemistry Analysis: A 1:300 dilution of this antibody detected Iba1/AIF1 in human spleen tissue.

其他说明

Concentration: Please refer to lot specific datasheet.

法律信息

ALEXA FLUOR is a trademark of Life Technologies

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储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Hao-Cheng Chang et al.
The Journal of biological chemistry, 299(1), 102728-102728 (2022-11-22)
Haploinsufficiency in retinoic acid induced 1 (RAI1) causes Smith-Magenis syndrome (SMS), a severe neurodevelopmental disorder characterized by neurocognitive deficits and obesity. Currently, curative treatments for SMS do not exist. Here, we take a recombinant adeno-associated virus (rAAV)-clustered regularly interspaced short

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