Merck
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P9287

Sigma-Aldrich

抗 小鼠 IgG（全分子）-R-藻红蛋白 山羊抗

affinity isolated antibody, buffered aqueous solution

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别名:
GoatAnti-Mouse IgG (whole molecule)–R-PE
MDL编号:
MFCD00162645

生物来源

goat

质量水平

200

偶联物

phycoerythrin (R-PE) conjugate

抗体形式

affinity isolated antibody

antibody product type

secondary antibodies

克隆

polyclonal

形式

buffered aqueous solution

technique(s)

indirect immunofluorescence: 1:20

运输

wet ice

储存温度

2-8°C

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P9287

抗 小鼠 IgG（全分子）-R-藻红蛋白 山羊抗

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P8172

Anti-Rabbit IgG (whole molecule), F(ab′)2 fragment−R-Phycoerythrin antibody produced in goat

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P9670

抗 小鼠 IgG（全分子）-R-藻红蛋白 山羊抗

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P9787

Anti-Goat IgG (whole molecule)−R-Phycoerythrin antibody produced in rabbit

conjugate

phycoerythrin (R-PE) conjugate

conjugate

phycoerythrin (R-PE) conjugate

conjugate

phycoerythrin (R-PE) conjugate

conjugate

phycoerythrin (R-PE) conjugate

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

clone

polyclonal

clone

polyclonal

clone

polyclonal

clone

polyclonal

form

buffered aqueous solution

form

buffered aqueous solution

form

buffered aqueous solution

form

buffered aqueous solution

technique(s)

indirect immunofluorescence: 1:20

technique(s)

indirect immunofluorescence: 1:20

technique(s)

indirect immunofluorescence: 1:20

technique(s)

indirect immunofluorescence: 1:20

一般描述

Immunoglobulin G (IgG) is a glycoprotein antibody that regulates immune responses such as phagocytosis and is also involved in the development of autoimmune diseases . Mouse IgGs have four distinct isotypes, namely, IgG1, IgG2a, IgG2b, and IgG3. IgG1 regulates complement fixation in mice . Anti-Mouse IgG (whole molecule)-R-Phycoerythrin antibody detects mouse IgG subclasses G1, G2a, G2b, and G3 and also reacts with mouse IgA and IgM by Ouchterlony Double Diffusion (ODD).

特异性

Binds all mouse Igs.

免疫原

Purified mouse IgG

应用

Anti-Mouse IgG (whole molecule)-R-Phycoerythrin antibody is suitable for use in flow cytometry . The antibody can also be used for indirect immunofluorescence (1:20).

外形

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 0.1 mM EDTA, 1 mM iodoacetamide, 1% bovine serum albumin and 15 mM sodium azide.

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.

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(F)

Not applicable

闪点(C)

Not applicable

Certificates of Analysis (COA)

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Structure and Function of Human and Murine Receptors for IgG
Unkeless, J.C., et al.
Annual Review of Immunology, 6, 251-281 (1989)
Karin Frischknecht et al.
Journal of vascular research, 43(4), 338-346 (2006-05-31)
The remarkable patency of internal mammary artery (MA) grafts compared to saphenous vein (SV) grafts has been related to different biological properties of the two blood vessels. We examined whether proliferation and apoptosis of vascular smooth muscle cells (VSMC) from
Leonardo Valdivieso-Torres et al.
Journal of virology, 90(6), 2971-2980 (2016-01-01)
Retargeting of gammaretroviral envelope proteins has shown promising results in the isolation of novel isolates with therapeutic potential. However, the optimal conditions required to obtain high-affinity retargeted envelope proteins with narrow tropism are not understood. This study highlights the advantage
Anne Rosbjerg et al.
Journal of innate immunity, 13(4), 211-224 (2021-03-30)
Activation of the complement system is mediated by the interaction between pathogens and pattern recognition molecules (PRMs); mannose-binding lectin (MBL), ficolins, and collectin-10/-11 from the lectin pathway and C1q from the classical pathway. Lectin pathway activation specifically depends on proteases
Benjamin P Roscoe et al.
Journal of molecular biology, 426(15), 2854-2870 (2014-05-28)
The complexity of biological interaction networks poses a challenge to understanding the function of individual connections in the overall network. To address this challenge, we developed a high-throughput reverse engineering strategy to analyze how thousands of specific perturbations (encompassing all
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