c-Oncogene Antibody Sampler Kit

    • c-Oncogene Antibody Sampler Kit -Elabscience
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    • c-Oncogene Antibody Sampler Kit -Elabscience
    • c-Oncogene Antibody Sampler Kit -Elabscience

      Catalog number:E-AB-K1677

      Size:
      • 9*20μL
      Qty:
      - +
      Price: $497

      Applications: WB

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      Product Includes

      Product name Specifications Application
      c-Fos Polyclonal Antibody 20μL WB,IHC-p,ELISA
      ABL1 Polyclonal Antibody 20μL WB,IHC-p,IF,ELISA
      JUN Polyclonal Antibody 20μL WB,IHC-p,IF,ELISA
      c-Kit Polyclonal Antibody 20μL WB,IHC-p,ELISA
      c-Myc Polyclonal Antibody 20μL WB,IHC-p,ELISA
      RAF1 Polyclonal Antibody 20μL WB,IHC-p,IF,ELISA
      N/H/K-Ras Polyclonal Antibody 20μL WB,IHC-p,ELISA
      c-Rel Polyclonal Antibody 20μL WB,IHC-p,ELISA
      c-SRC Polyclonal Antibody 20μL WB,IHC-p,IF,ELISA
      Goat Anti-Rabbit IgG (H+L)(peroxidase/HRP conjugated) 120μL WB,IHC,ELISA

      Product Photos

      Western Blot analysis of HT29 cells using c-Fos Polyclonal Antibody at dilution of 1:500.

      Western Blot analysis of 293 cells using ABL1 Polyclonal Antibody at dilution of 1:1000.

      Western Blot analysis of HuvEc cells using JUN Polyclonal Antibody at dilution of 1:500.

      Western Blot analysis of 453 cells using c-Kit Polyclonal Antibody at dilution of 1:500.

      Western Blot analysis of Jurkat cells with c-Myc Polyclonal Antibody.

      Western Blot analysis of Hela cells using RAF1 Polyclonal Antibody at dilution of 1:1000.

      Western Blot analysis of 293T cells using N/H/K-Ras Polyclonal Antibody at dilution of 1:1000.

      Western Blot analysis of COLO205 cells with c-Rel Polyclonal Antibody.

      Western Blot analysis of Hela cells using c-Src Polyclonal Antibody at dilution of 1:2000.

      Product description

      The c-Oncogene Antibody Sampler Kit provides an economical means of evaluating total levels of various oncogenic proteins. The kit contains enough primary and secondary antibodies to perform two Western blot experiments.

      Background

      The regulation of cell growth, differentiation and programmed death is coordinated by several sets of proteins that comprise essential signal transduction pathways. Many of these key regulatory proteins are encoded by proto-oncogenes, which can be activated (altered) to change the typical cell program to one of abnormal cell growth and unregulated development. Proteins encoded by proto-oncogenes include growth factors and other ligands, receptor proteins, tyrosine kinases, various regulatory proteins (i.e. GTPases) and transcription factors. Together these proteins comprise the basic elements of cell signaling pathways; altered expression or mutation of one or more of these components can lead to oncogenic growth. Non-receptor (i.e. cytoplasmic, nuclear) tyrosine kinases such as c-Abl and Src play key roles in the regulation of cell proliferation, differentiation, apoptosis, cell adhesion and stress responses. Alteration of the corresponding c-Abl and Src proto-oncogenes is associated with oncogenesis; Abl1-BCR gene translocations result in chronic myelogenous leukemia (CML) while constitutively active Src is seen in some patients with colon cancer and altered Src expression is seen in a wide array of cancers. Regulation of Raf tyrosine kinase by Ras GTPase controls downstream kinases in the MEK/MAPK signaling pathway. Activation of the Ras and Raf proto-oncogenes are common in human cancers and both proteins are seen as potential therapeutic targets. The receptor tyrosine kinase c-Kit plays a critical role in activation and growth of hematopoietic stem cells; mutations that inhibit c-Kit kinase activity are associated with a variety of developmental disorders while mutations producing constitutively active c-Kit can result in mastocytosis and gastrointestinal stromal tumors. The alteration of key transcription factors such as c-Fos, c-Jun, c-Myc and c-Rel that are normally responsible for regulating cell and tissue growth, differentiation and the inflammation/immune response, can also result in unregulated, oncogenic cell growth.

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