• merck millipore,默克密理博,MAB10005,Anti-ABCA1 Antibody, clone AB.H10
  • merck millipore,默克密理博,MAB10005,Anti-ABCA1 Antibody, clone AB.H10

    产品名称:Anti-ABCA1 Antibody, clone AB.H10
    产品型号:MAB10005
    This Anti-ABCA1 Antibody, clone AB.H10 is validated for use in ELISA, IP, WB, IH(P) for the detection of ABCA1.

    merck millipore,默克密理博,MAB10005,Anti-ABCA1 Antibody, clone AB.H10

  • 产品介绍
  • merck millipore,默克密理博,MAB10005,Anti-ABCA1 Antibody, clone AB.H10

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    M, Ch, HWB, ELISAMPurifiedMonoclonal Antibody
    描述
    产品目录编号 MAB10005
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-ABCA1 Antibody, clone AB.H10
    Alternate Names
    • Cholesterol efflux regulatory protein
    • ABC-1
    • ATP-binding cassette transporter 1
    背景信息 Mutations in the ABCA1 gene are associated with Tangier disease (TD). TD is an autosomal recessive disorder results from an absence of plasma HDL, cholesterol ester depositing in the reticulo-endothelial system and disorders in cellular lipid trafficking. It is expressed on the plasma membrane and the Golgi complex, and is regulated by cholesterol flux. Regulation of the cholesterol flux between HDL and macrophages is competitive between ABCA1 and SR-BI.
    产品信息
    格式 Purified
    演示 Presented as a liquid in PBS, pH 7.4 with 0.05% sodium azide.
    应用
    应用 This Anti-ABCA1 Antibody, clone AB.H10 is validated for use in ELISA, IP, WB, IH(P) for the detection of ABCA1.
    主要应用
    • Western Blotting
    • ELISA
    应用说明 ELISA
    Immunohistochemistry (Paraffin): 5 μg/mL. Perform heat mediated antigen retrieval in sodium citrate buffer (pH 6), before commencing with IHC staining protocol. Amplification with biotin-streptavidin may be required.
    Immunoprecipitation
    Western Blot: 1 μg/mL. Predicted molecular weight: 254 kDa.

    Optimal working dilutions must be determined by end user.
    生物信息
    免疫原品种 Recombinant fragment, corresponding to amino acids 1800-2260 of Human ABCA1.
    克隆 AB.H10
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Mouse
    特异性 Recognize specifically ABCA1 from human, mouse, and chicken.
    同种型 IgG1
    品种反应性 MouseChickenHuman
    抗体类型 Monoclonal Antibody
    Entrez基因编号
    • NM_005502.2
    Entrez基因汇总 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. With cholesterol as its substrate, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in this gene have been associated with Tangier's disease and familial high-density lipoprotein deficiency.
    基因符号
    • FLJ14958
    • ABCA1
    • MGC165011
    • HDLDT1
    • ABC1
    • TGD
    • CERP
    • membrane-bound
    • TD
    • ABC-1
    • MGC164864
    UniProt编号
    • O95477
    UniProt汇总 FUNCTION: SwissProt: O95477 # cAMP-dependent and sulfonylurea-sensitive anion transporter. Key gatekeeper influencing intracellular cholesterol transport.
    SIZE: 2261 amino acids; 254286 Da
    SUBUNIT: Interacts with MEGF10.
    TISSUE SPECIFICITY: Widely expressed, but most abundant in macrophages.
    DOMAIN: SwissProt: O95477 Multifunctional polypeptide with two homologous halves, each containing an hydrophobic membrane-anchoring domain and an ATP binding cassette (ABC) domain.
    PTM: Phosphorylation on Ser-2054 regulates phospholipid efflux.
    DISEASE: SwissProt: O95477 # Defects in ABCA1 are a cause of high density lipoprotein deficiency type 1 (HDLD1) [MIM:205400]; also known as analphalipoproteinemia or Tangier disease (TGD). HDLD1 is a recessive disorder characterized by absence of high density lipoprotein (HDL) cholesterol from plasma, accumulation of cholesteryl esters, premature coronary artery disease (CAD), hepatosplenomegaly, recurrent peripheral neuropathy and progressive muscle wasting and weakness. & Defects in ABCA1 are a cause of high density lipoprotein deficiency type 2 (HDLD2) [MIM:604091]; also known as familial hypoalphalipoproteinemia (FHA). HDLD2 is inherited as autosomal dominant trait. It is characterized by moderately low HDL cholesterol, predilection toward premature coronary artery disease (CAD) and a reduction in cellular cholesterol efflux.
    SIMILARITY: Belongs to the ABC transporter family. ABCA subfamily. & Contains 2 ABC transporter domains.
    产品使用声明
    使用声明
    • 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.
    储存和货运信息
    存储条件 Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing. Aliquot will be stable at 4°C for 3 months.
    包装信息
    数量 100 µg

    merck millipore,默克密理博,MAB10005,Anti-ABCA1 Antibody, clone AB.H10

上一件merck millipore产品:merck millipore,默克密理博,MAB1217F-K,Anti-Fmc-7 B-Cell Lymphocyte Marker, clone Fmc-7, FITC conjugated (1mL)
下一件merck millipore产品:merck millipore,默克密理博,07-643,Anti-Scrib Antibody



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