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L-Myc (E3M5P) Rabbit mAb #76266

Filter:
  • WB
  • IP
  • ChIP
Western Blotting Image 1: L-Myc (E3M5P) Rabbit mAb
Western blot analysis of various cell lines using L-Myc (E3M5P) Rabbit mAb (upper), c-Myc (E5Q6W) Rabbit mAb #18583 (upper-middle), N-Myc (D4B2Y) Rabbit mAb #51705 (lower-middle), and GAPDH (D16H11) XP® Rabbit mAb #5174 (lower). The cell type specificity for each of the Myc family members is predicted from RNAseq data and confirms the specificity of the antibodies. NCI-H1963 cells express both wild-type and an RLF-L-Myc fusion protein resulting from intrachromosomal rearrangement.

To Purchase # 76266

Supporting Data

REACTIVITY H
SENSITIVITY Endogenous
MW (kDa) 62
Source/Isotype Rabbit IgG
Application Key:
  • WB-Western Blotting 
  • IP-Immunoprecipitation 
  • ChIP-Chromatin Immunoprecipitation 
Species Cross-Reactivity Key:
  • H-Human 
  • Related Products

Product Information

Product Usage Information

For optimal ChIP results, use 10 μl of antibody and 10 μg of chromatin (approximately 4 × 106 cells) per IP. This antibody has been validated using SimpleChIP® Enzymatic Chromatin IP Kits.

Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:200
Chromatin IP 1:50

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 μg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at -20ºC. Do not aliquot the antibody.

Protocol

Specificity / Sensitivity

L-Myc (E3M5P) Rabbit mAb recognizes endogenous levels of total L-Myc protein. Cross-reactivity was not observed with other family members.

Species Reactivity:

Human

Source / Purification

Monoclonal antibody is produced by immunizing animals with recombinant protein specific to the carboxy terminus of human L-Myc protein. The epitope has been mapped to residues surrounding Thr190.

Background

Members of the Myc/Max/Mad network function as transcriptional regulators with roles in various aspects of cell behavior, including proliferation, differentiation, and apoptosis (1). These proteins share a common basic-helix-loop-helix leucine zipper (bHLH-ZIP) motif required for dimerization and DNA-binding. Max was originally discovered based on its ability to associate with c-Myc and found to be required for the ability of Myc to bind DNA and activate transcription (2). Subsequently, Max has been viewed as a central component of the transcriptional network, forming homodimers as well as heterodimers with other members of the Myc and Mad families (1). The association between Max and either Myc or Mad can have opposing effects on transcriptional regulation and cell behavior (1). The Mad family consists of four related proteins; Mad1, Mad2 (Mxi1), Mad3, and Mad4, and the more distantly related members of the bHLH-ZIP family, Mnt and Mga. Like Myc, the Mad proteins are tightly regulated with short half-lives. In general, Mad family members interfere with Myc-mediated processes, such as proliferation, transformation, and prevention of apoptosis by inhibiting transcription (3,4).

The Myc family is comprised of c-Myc, N-Myc, and L-Myc with often distinct patterns of expression during development as well as cancer (5). Amplification of each of the family members in cancer is frequently mutually exclusive with c-Myc being the most widely studied and most commonly amplified. N-Myc amplification, on the other hand, is found predominantly in neuroblastomas, and L-Myc amplification has been described in small cell lung cancer (SCLC) (6). Amplification of L-Myc in SCLC may result from chromosomal rearrangement between the rlf and MYCL genes (7). L-Myc expression by dendritic cells may be required for optimal T cell priming (8).
For Research Use Only. Not For Use In Diagnostic Procedures.
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