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LDL receptor Recombinant Rabbit mAb (SDT-057-57)

Low-density lipoprotein receptor,LDLR

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B2054
规格
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    LDL Receptor
  • 分子别名

    Low-density lipoprotein receptor, LDLR
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Golgi Apparatus, Lysosome, Endosome, Plasma Membrane
  • Accession

    P01130
  • 克隆号

    SDT-057-57
  • 抗体类型

    Rabbit mAb
  • 反应种属 ?

    Hu, Ms, Rt
  • 预测反应种属
    (反应种属缩写表)

    Bv, Rb
  • 纯化方式

    Protein A
  • 浓度

    0.25mg/ml
  • 性状

    Liquid
  • 缓冲体系

    PBS, 40% Glycerol, 0.05%BSA, 0.03% Proclin 300
  • 储存条件

    12 months from date of receipt / reconstitution, -20 °C as supplied

  • 应用

    IHC-P ?

    WB

  • 稀释度

    应用 稀释度 推荐种属
    IHC-P 1:1000 Hu, Ms, Rt
    WB 1:500 Hu, Ms, Rt
背景介绍
  • The low density lipoprotein receptor (LDL R) is the founding member of the LDL R family of scavenger receptors.Binds LDL, the major cholesterol-carrying lipoprotein of plasma, and transports it into cells by endocytosis.LDLR is ubiquitously expressed and is a key receptor for maintaining cholesterol homeostasis in mammals. LDLR-mediated endocytosis is essential for lipoprotein and lipid metabolism.Impaired LDLR function by genetic mutations results in a condition with extremely elevated serum LDL levels and early onset atherosclerosis known as familial hypercholesterolemia (FH).

  • 免疫印迹

    • WB result of LDL-receptor Rabbit mAb

      Primary antibody: LDL-receptor Rabbit mAb at 1/500 dilution
      Lane 1: LNCaP whole cell lysate 20 µg
      Lane 2: HEK293 whole cell lysate 20 µg
      Lane 3: PC-3 whole cell lysate 20 µg
      Lane 4: HepG2 whole cell lysate 20 µg
      Lane 5: Hela whole cell lysate 20 µg
      Low expression control: HEK293 whole cell lysate

      low expression control: LNCaP whole cell lysate

      Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 140 kDa
      Observed MW: 140 kDa
      Exposure time: 120s

    • WB result of LDL-receptor Rabbit mAb

      Primary antibody: LDL-receptor Rabbit mAb at 1/500 dilution
      Lane 1: RAW264.7 whole cell lysate 20 µg
      Lane 2: rat liver whole cell lysate 20 µg

      Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 140 kDa
      Observed MW: 140 kDa
      Exposure time: 180s

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded human liver.

      Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded human liver cancer.

      Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded mouse liver.

      Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded mouse stomach.

      Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded rat liver.

      Anti-LDL receptor antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use.

      Counterstained with hematoxylin.

      Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

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