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Recombinant Actin 抗体

The 兔 单克隆 anti-Actin antibody (ABIN6942041) specifically detects Actin in WB, IF, IP, ICC, FACS, IHC (p) 和 IHC (fro). The antibody is reactive with 人, 大鼠 和 小鼠 samples.
产品编号 ABIN6942041
发货至: 中国
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Our Local Distributor

中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Recombinant Actin 抗体 (ABIN6942041)

抗原

See all Actin 抗体
Actin

抗体类型

Recombinant Antibody

适用

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人, 大鼠, 小鼠

宿主

  • 127
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  • 2
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克隆类型

  • 92
  • 80
单克隆

标记

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This Actin antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP), Immunocytochemistry (ICC), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 原理

    Actin Recombinant Antibody

    交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    Full length protein

    亚型

    IgG
  • 应用备注

    WB(), IHC-P(1:200-400), IHC-F(1:100-500), IP(1-2 μg), IF(), Flow-Cyt(1 μg/Test), ICC/IF(1:50-100)

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    0.01M TBS ( pH 7.4), 1 % BSA, 0.02 % Proclin 300, and 50 % Glycerol

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C for 12 months.

    有效期

    12 months
  • 抗原

    Actin

    背景

    Synonyms: Actin, alpha skeletal muscle, Alpha-actin-1, ACTA1

    Background: The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects. [provided by RefSeq, Jul 2008]

    基因ID

    58

    UniProt

    P68133
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