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Merck
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76085

Sigma-Aldrich

Anti-Mouse IgG - Atto 594 antibody produced in goat

~1 mg/mL protein, affinity isolated antibody

别名:

Atto 594 - goat-Anti-mouse IgG

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About This Item

UNSPSC代码:
12352203
NACRES:
NA.46

生物来源

goat

偶联物

Atto 594 conjugate

抗体形式

affinity isolated antibody

抗体产品类型

secondary antibodies

克隆

polyclonal

包含

50% glycerol as stabilizer

种属反应性

mouse

浓度

~1 mg/mL protein

荧光

λex 603 nm; λem 625 nm in PBS

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

相关类别

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.
Affinity isolated antigen specific antibody is purified from goat anti-mouse IgG antiserum to remove essentially all goat serum proteins, including immunoglobulin. Goat anti-mouse IgG associates with mouse IgGs.

免疫原

purified mouse IgG

应用

Atto 594-goat anti-mouse IgG can be used for fluorescence-based immunoassays.

分析说明

unconjugated dye ≤5% of total fluorescence; dye-to-protein ratio ≥2

法律信息

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

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 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCL0327
BCCJ5729
BCCG6586
BCCF3697
BCCD4078

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Charles Bou-Nader et al.
Cell host & microbe, 29(9), 1421-1436 (2021-08-14)
The HIV-1 virion structural polyprotein, Gag, is directed to particle assembly sites at the plasma membrane by its N-terminal matrix (MA) domain. MA also binds to host tRNAs. To understand the molecular basis of MA-tRNA interaction and its potential function
Mirko Cortese et al.
Cell host & microbe, 28(6), 853-866 (2020-11-28)
Pathogenesis induced by SARS-CoV-2 is thought to result from both an inflammation-dominated cytokine response and virus-induced cell perturbation causing cell death. Here, we employ an integrative imaging analysis to determine morphological organelle alterations induced in SARS-CoV-2-infected human lung epithelial cells.
Paola Muttathukunnel et al.
Proceedings of the National Academy of Sciences of the United States of America, 119(45), e2119044119-e2119044119 (2022-11-03)
Robust neural information transfer relies on a delicate molecular nano-architecture of chemical synapses. Neurotransmitter release is controlled by a specific arrangement of proteins within presynaptic active zones. How the specific presynaptic molecular architecture relates to postsynaptic organization and how synaptic
Anu G Nair et al.
Cell reports, 37(11), 110105-110105 (2021-12-16)
Presynaptic homeostatic plasticity (PHP) stabilizes synaptic transmission by counteracting impaired neurotransmitter receptor function through neurotransmitter release potentiation. PHP is thought to be triggered by impaired receptor function and to involve a stereotypic signaling pathway. However, here we demonstrate that different
Krzysztof Marycz et al.
International journal of nanomedicine, 16, 6049-6065 (2021-09-14)
Healing of osteoporotic defects is challenging and requires innovative approaches to elicit molecular mechanisms promoting osteoblasts-osteoclasts coupling and bone homeostasis. Cytocompatibility and biocompatibility of previously characterised nanocomposites, i.e Ca5(PO4)3OH/Fe3O4 (later called nHAp/IO) functionalised with microRNAs (nHAp/IO@miR-21/124) was tested. In vitro
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