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QPRT Recombinant Rabbit mAb (S-1228-31)

QPRT Recombinant Rabbit mAb (S-1228-31)

货号: S0B0773
价格: 600
规格: 25μl
介绍: -
其他: -
产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    QPRT
  • 分子别名

    Nicotinate-nucleotide pyrophosphorylase [carboxylating], Quinolinate phosphoribosyltransferase [decarboxylating]
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Cytoplasm
  • Accession

    Q15274
  • 克隆号

    S-1228-31
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 应用

    IHC-P, WB, IP
  • 反应种属 ?

    Hu
  • 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

稀释度
应用 稀释度
WB 1:1000
IHC-P 1:1000
IP 1:50
背景介绍
  • QPRT, also known as Quinolinate Phosphoribosyltransferase, is an enzyme that catalyzes the conversion of quinolinic acid to nicotinic acid mononucleotide (NAMN) in the biosynthetic pathway of nicotinamide adenine dinucleotide (NAD+). This reaction involves the attachment of phosphoribosyl pyrophosphate (PRPP) to quinolinic acid, forming NAMN and pyrophosphate. QPRT plays a crucial role in maintaining the cellular NAD+ pool, which is essential for cellular metabolism, DNA repair, and other cellular functions. Abnormalities in QPRT activity or expression have been linked to various diseases, including cancer, neurodegenerative disorders, and metabolic diseases. In cancer, QPRT is often overexpressed, and its activity may contribute to tumor growth and progression. This is because NAD+ is a cofactor for many enzymes involved in cellular metabolism, including those that regulate glycolysis, fatty acid synthesis, and oxidative phosphorylation. By maintaining a high level of NAD+, QPRT may support the metabolic demands of rapidly proliferating tumor cells.

  • 免疫印迹

    • WB result of QPRT Recombinant Rabbit mAb
      Primary antibody: QPRT Recombinant mAb at 1/1000 dilution
      Lane 1: MDA-MB-231 whole cell lysate 20 µg
      Lane 2: Jurkat whole cell lysate 20 µg
      Lane 3: HeLa whole cell lysate 20 µg
      Lane 4: MCF7 whole cell lysate 20 µg
      Negative control: MDA-MB-231 whole cell lysate
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 31 kDa
      Observed MW: 37 kDa

  • 免疫沉淀

    • QPRT Rabbit mAb at 1/50 dilution (1 µg) immunoprecipitating QPRT in 0.4 mg HepG2 whole cell lysate.
      Western blot was performed on the immunoprecipitate using QPRT Rabbit mAb at 1/1000 dilution.
      Secondary antibody (HRP) for IP was used at 1/1000 dilution.
      Lane 1: HepG2 whole cell lysate 20 µg (Input)
      Lane 2: QPRT Rabbit mAb IP in HepG2 whole cell lysate
      Lane 3: Rabbit monoclonal IgG IP in HepG2 whole cell lysate
      Predicted MW: 31 kDa 
      Observed MW: 37 kDa

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded human kidney. Anti- QPRT antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & 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- QPRT antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & 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 testis. Anti- QPRT antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & 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 tonsil. Anti- QPRT antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & 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 prostatic hyperplasia. Anti- QPRT antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & 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 colon cancer. Anti- QPRT antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & 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 lung adenocarcinoma. Anti- QPRT antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & 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.