电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

APOA1 抗体

This anti-APOA1 antibody is a 兔 多克隆 antibody detecting APOA1 in WB, ICC, IHC (p) 和 IF. Suitable for 人.
产品编号 ABIN7467691
发货至: 中国

Quick Overview for APOA1 抗体 (ABIN7467691)

抗原

See all APOA1 抗体
APOA1 (Apolipoprotein A-I (APOA1))

适用

  • 122
  • 39
  • 24
  • 12
  • 12
  • 12
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1

宿主

  • 98
  • 61
  • 19
  • 6
  • 3
  • 3
  • 2

克隆类型

  • 124
  • 67
多克隆

标记

  • 102
  • 34
  • 15
  • 11
  • 8
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This APOA1 antibody is un-conjugated

应用范围

  • 128
  • 80
  • 66
  • 37
  • 36
  • 20
  • 12
  • 8
  • 8
  • 8
  • 8
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Full length human Apolipoprotein A1 Recombinant protein.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:20000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.58 mg/mL

    缓冲液

    1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300

    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

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    APOA1 (Apolipoprotein A-I (APOA1))

    别名

    apolipoprotein A1

    背景

    Apolipoprotein A1 , apo(a),This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The protein promotes cholesterol efflux from tissues to the liver for excretion, and it is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. [provided by RefSeq]

    分子量

    31 kDa

    基因ID

    335

    UniProt

    P02647

    途径

    Regulation of Lipid Metabolism by PPARalpha, Production of Molecular Mediator of Immune Response, Lipid Metabolism
You are here:
Chat with us!