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LDLR 抗体 (AA 29-205)

This anti-LDLR antibody is a 小鸡 多克隆 antibody detecting LDLR in WB. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN2467854
发货至: 中国

Quick Overview for LDLR 抗体 (AA 29-205) (ABIN2467854)

抗原

See all LDLR 抗体
LDLR (Low Density Lipoprotein Receptor (LDLR))

适用

  • 89
  • 42
  • 28
  • 17
  • 16
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
人, 小鼠, 大鼠

宿主

  • 81
  • 15
  • 4
小鸡

克隆类型

  • 76
  • 23
  • 1
多克隆

标记

  • 59
  • 7
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LDLR antibody is un-conjugated

应用范围

  • 70
  • 41
  • 30
  • 29
  • 16
  • 14
  • 13
  • 11
  • 8
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 16
    • 8
    • 6
    • 5
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 29-205

    纯化方法

    Antigen affinity-purified
  • 应用备注

    LDL-R antibody can be used for the detection of LDL-R by Western blot, may also work for IHC and ICC.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    Phosphate-Buffered Saline. No preservatives added.

    储存液

    Without preservative

    注意事项

    As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

    储存条件

    4 °C/-20 °C

    储存方法

    LDLR antibody can be stored at 4 °C for short term (weeks). Long term storage should be at -20 °C.
  • 抗原

    LDLR (Low Density Lipoprotein Receptor (LDLR))

    别名

    LDLR

    背景

    Low density lipoprotein receptor. The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. Low density lipoprotein (LDL) is normally bound at the cell membrane and taken into the cell ending up in lysosomes where the protein is degraded and the cholesterol is made available for repression of microsomal enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase, the rate-limiting step in cholesterol synthesis. At the same time, a reciprocal stimulation of cholesterol ester synthesis takes place. Mutations in this gene cause the autosomal dominant disorder, familial hypercholesterolemia.

    分子量

    95.4 kDa (calculated)

    基因ID

    3949

    NCBI登录号

    NP_000518

    UniProt

    P01130

    途径

    Hepatitis C, Lipid Metabolism
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