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4E-BP1/2/3 抗体 (pThr45)

This anti-4E-BP1/2/3 antibody is a 小鼠 单克隆 antibody detecting 4E-BP1/2/3 in WB. Suitable for 人 和 大鼠.
产品编号 ABIN6942017
发货至: 中国

Quick Overview for 4E-BP1/2/3 抗体 (pThr45) (ABIN6942017)

抗原

4E-BP1/2/3

适用

人, 大鼠

宿主

  • 7
小鼠

克隆类型

  • 7
单克隆

标记

  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This 4E-BP1/2/3 antibody is un-conjugated

应用范围

Western Blotting (WB)

克隆位点

3G2
  • 抗原表位

    pThr45

    交叉反应

    人, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    Synthetic peptide derived from human 4E-BP1/2/3 (Thr 45), around 35-55aa.

    亚型

    IgG2a
  • 应用备注

    WB 1:300-5000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 1xTBS ( pH 7.4), 1 % BSA, 40 %Glycerol and 0.05 % Sodium Azide.

    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

    4E-BP1/2/3

    背景

    Synonyms: ABCA1 phospho S2054, p-ABCA1 phospho S2054, ATP binding cassette transporter A1, ABC 1, ABC Transporter 1, ABC1, ABCA 1, ABCA1, ATP binding Cassette 1, ATP binding cassette sub family A ABC1 member 1, ATP binding cassette sub family A member 1, ATP binding cassette sub-family A member 1, ATP binding Cassette Transporter 1, ATP-binding Cassette 1, ATP-binding Cassette Transporter 1, CERP, Cholesterol Efflux Regulatory Protein, FLJ14958, HDLDT1, Membrane bound, MGC164864, MGC165011, TD, TGD, ABCA1_HUMAN.

    Background: The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. In humans, this protein functions as a cholesterol efflux pump in the cellular lipid removal pathway. Mutations in the human gene have been associated with Tangier's disease and familial high-density lipoprotein deficiency.

    基因ID

    19

    UniProt

    O95477
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