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Merck
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重要文件

76085

Sigma-Aldrich

Anti-Mouse IgG - Atto 594 antibody produced in goat

~1 mg/mL protein, affinity isolated antibody

同義詞:

Atto 594 - goat-Anti-mouse IgG

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.46

生物源

goat

品質等級

共軛

Atto 594 conjugate

抗體表格

affinity isolated antibody

抗體產品種類

secondary antibodies

無性繁殖

polyclonal

包含

50% glycerol as stabilizer

物種活性

mouse

濃度

~1 mg/mL protein

螢光

λex 603 nm; λem 625 nm in PBS

運輸包裝

wet ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

一般說明

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

應用

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

分析報告

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

法律資訊

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

免責聲明

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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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves


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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.
Barbara Storti et al.
Computational and structural biotechnology journal, 19, 6140-6156 (2021-11-09)
We exploited a multi-scale microscopy imaging toolbox to address some major issues related to SARS-CoV-2 interactions with host cells. Our approach harnesses both conventional and super-resolution fluorescence microscopy and easily matches the spatial scale of single-virus/cell checkpoints. After its validation
Edward M Courchaine et al.
Cell, 184(14), 3612-3625 (2021-06-12)
Biomolecular condensation is a widespread mechanism of cellular compartmentalization. Because the "survival of motor neuron protein" (SMN) is implicated in the formation of three different membraneless organelles (MLOs), we hypothesized that SMN promotes condensation. Unexpectedly, we found that SMN's globular
Shun Hang Chan et al.
Developmental cell, 49(6), 867-881 (2019-06-19)
The awakening of the genome after fertilization is a cornerstone of animal development. However, the mechanisms that activate the silent genome after fertilization are poorly understood. Here, we show that transcriptional competency is regulated by Brd4- and P300-dependent histone acetylation

文章

Immunoblotting (Western blot transfer) is a common technique in modern proteomics research.

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