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Merck
CN

MAB1570

Anti-NMDAR1 Antibody, CT, C2 cassette, clone 2C6.2

clone 2C6.2, Chemicon®, from mouse

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关于此项目

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41
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生物来源

mouse

抗体形式

purified immunoglobulin

抗体产品类型

primary antibodies

克隆

2C6.2, monoclonal

种属反应性

rat

制造商/商品名称

Chemicon®

技术

immunohistochemistry: suitable
western blot: suitable

同位素/亚型

IgG2b

UniProt登记号

运输

wet ice

靶向翻译后修饰

unmodified

基因信息

rat ... Grin1(24408)

免疫原

Epitope: C-terminus, C2 cassette
Synthetic peptide (LQNQKDTVLPRRAIEREEGQLQLCSRHRES) corresponding to the C-terminus of rat NMDA receptor subunit.

应用

Anti-NMDAR1 Antibody, C-terminus, C2 cassette, clone 2C6.2 is an antibody against NMDAR1 for use in IH & WB.
Research Category
Neuroscience
Research Sub Category
Neurotransmitters & Receptors
Western blot: 1:100-1:500

Immunohistochemistry: 1:100-1:500 using paraformaldehyde or paraformaldehyde/glutaraldehyde fixed tissue with light and electron microscopy.

Optimal working dilutions must be determined by the end user.

生化/生理作用

NMDAR1, C-terminal, C2 cassette

外形

Format: Purified
Purified immunoglobulin. Liquid in 0.02M Phosphate buffer, 0.25 M NaCl with 0.1% sodium azide.

制备说明

Maintain at 2-8°C in undiluted aliquots for up to 6 months.

其他说明

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

法律信息

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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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储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


分析证书(COA)

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Tom J Phillips et al.
Scientific reports, 7(1), 9079-9079 (2017-08-24)
Some neuropsychiatric disease, including schizophrenia, may originate during prenatal development, following periods of gestational hypoxia and placental oxidative stress. Here we investigated if gestational hypoxia promotes damaging secretions from the placenta that affect fetal development and whether a mitochondria-targeted antioxidant

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