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4E-BP1/2/3 抗体 (pThr45)

适用: 人, 大鼠 WB 宿主: 小鼠 Monoclonal 3G2 unconjugated
产品编号 ABIN6942017
发货至: 中国
  • 抗原 See all 4E-BP1/2/3 products
    4E-BP1/2/3
    抗原表位
    pThr45
    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)
    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.
    克隆位点
    3G2
    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
    Abstract
    4E-BP1/2/3 产品
    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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