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Pklr Recombinant Rabbit mAb (S-4114-40)

Pyruvate kinase PKLR,Pyruvate kinase 1,Pyruvate kinase isozymes L/R,R-type/L-type pyruvate kinase,Red cell/liver pyruvate kinase,PK1,PKL,PKLR

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B6976
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产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    Pklr
  • 分子别名

    Pyruvate kinase PKLR; Pyruvate kinase 1; Pyruvate kinase isozymes L/R; R-type/L-type pyruvate kinase; Red cell/liver pyruvate kinase; PK1; PKL; PKLR
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Cytoplasm
  • Accession

    P30613
  • 克隆号

    S-4114-40
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Hu, Ms, Rt
  • 阳性样本

    Mouse liver, rat liver
  • 纯化方式

    Protein A
  • 浓度

    0.5 mg/ml
  • 标记

    Unconjugated
  • 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

    IF ?

  • 稀释度

    应用 稀释度 推荐种属
    WB 1:1000 Ms, Rt
    IHC-P 1:1000 Hu, Ms, Rt
    IF 1:500 Hu, Ms
背景介绍
  • Pyruvate kinase liver and red blood cell (PKLR) is a critical metabolic enzyme encoded by the PKLR gene, primarily expressed in the liver and erythrocytes, where it catalyzes the final, irreversible step of glycolysis by transferring a phosphate group from phosphoenolpyruvate (PEP) to adenosine diphosphate (ADP), thereby generating pyruvate and ATP. This enzyme exists as distinct isoforms due to alternative promoter usage and tissue-specific splicing: the L-type isoform in the liver is allosterically regulated by hormones and metabolites like fructose-1,6-bisphosphate to maintain glucose homeostasis, while the R-type isoform in red blood cells ensures sufficient ATP production to preserve membrane integrity and cellular deformability. Mutations in the PKLR gene are the primary cause of hereditary nonspherocytic hemolytic anemia, as deficient enzymatic activity leads to ATP depletion in red blood cells, resulting in premature cell destruction, chronic hemolysis, and compensatory reticulocytosis, highlighting its indispensable role in both systemic energy metabolism and erythrocyte survival.

  • 免疫印迹

    • WB result of Pklr Recombinant Rabbit mAb
      Primary antibody: Pklr Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: mouse skeletal muscle lysate 20 µg
      Lane 2: mouse liver lysate 20 µg
      Low expression control: mouse skeletal muscle lysate
      Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 62 kDa
      Observed MW: 60 kDa

    • WB result of Pklr Recombinant Rabbit mAb
      Primary antibody: Pklr Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: rat skeletal muscle lysate 20 µg
      Lane 2: rat liver lysate 20 µg
      Low expression control: rat skeletal muscle lysate
      Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 62 kDa
      Observed MW: 60 kDa

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded human kidney. Anti-Pklr antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (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. Anti-Pklr antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded human skeletal muscle. Anti-Pklr antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (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 kidney. Anti-Pklr antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded mouse skeletal muscle. Anti-Pklr antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (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 kidney. Anti-Pklr antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded rat skeletal muscle. Anti-Pklr antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

  • 免疫荧光

    • IF shows positive staining in paraffin-embedded human liver. Anti-Pklr antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • Negative control: IF shows negative staining in paraffin-embedded human skeletal muscle. Anti-Pklr antibody was used at 1/500 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded mouse liver. Anti-Pklr antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • Negative control: IF shows negative staining in paraffin-embedded mouse skeletal muscle. Anti-Pklr antibody was used at 1/500 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

  • 组织表达图谱

    • Expression of Pklr in tumor tissues.

    • Expression of Pklr in human tissues.

    • Expression of Pklr in mouse & rat tissues.

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