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Enzolifesciences/c-Myc (human) monoclonal antibody (6A10)/ALX-804-632-L001/1ml

Product Specification:

Alternative Name:Myc proto-oncogene, Transcription factor p64
Clone:6A10
Host:Rat
Isotype:IgG2a
Immunogen:Human c-Myc (aa 1-262).
UniProt ID:P01106
Species reactivity:Human
Applications:ICC, IP, WB
Recommended Dilutions/Conditions:Immunocytochemistry (1:10)Immunoprecipitation (1:10)Western Blot (1:50)Suggested dilutions/conditions may not be available for all applications.Optimal conditions must be determined individually for each application.
Formulation:Liquid. Tissue culture supernatant (TCS) containing 0.1% sodium azide.
Use/Stability:Stable for at least 1 yearwhen stored at +4°C.
Handling:Avoid freeze/thaw cycles. After opening, prepare aliquots and store at -20°C.
Shipping:Shipped on Blue Ice
Long Term Storage:+4°C
Scientific Background:Myc proteins are important regulators of cell behaviour and work as transcription factors that belong to the basic region/helix-loop-helix/leucine zipper family of DNA binding proteins. To regulate its target genes, Myc recruits several different cofactors (e.g. PARP-10). They control a variety of cellular functions including protein synthesis, cell cycle progression, and apoptosis, thereby modulating cell growth and proliferation, differentiation, and survivial of cells. The family of myc genes includes B-myc, L-myc, N-myc and s-myc; however only c-myc, L-myc and N-myc have neoplastic potential. The c-Myc gene was discovered as the cellular homolog of the retroviral v-myc oncogene. It is a proto-oncogene, whereas the deregulated expression of c-Myc is observed in the majority of human and animal tumors often with poor prognosis. The proto-oncogene c-Myc is implicated in various physiological processes; cell growth, proliferation, loss of differentiation and cell death (apoptosis). It also has been implicated in the loss and dysfunction of insulin-producing beta cells in diabetes. Studies in mice suggest that c-Myc has unexpected functions during both self-renewal and the differentiation of stem and early progenitor cells. c-Myc activity is normally tightly controlled by external signals including growth factors, mitogens and β-catenin which promote, and factors as TGF-beta which inhibit.