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Anti-phospho-c-Myc (Ser347), Cat. No. ABC1461, is a rabbit polyclonal antibody that detects c-Myc phosphorylated on serine 347 and is tested for use in Peptide Inhibition Assay and Western Blotting.
More>>Anti-phospho-c-Myc (Ser347), Cat. No. ABC1461, is a rabbit polyclonal antibody that detects c-Myc phosphorylated on serine 347 and is tested for use in Peptide Inhibition Assay and Western Blotting. Less<<
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Übersicht
Replacement Information
Description
Catalogue Number
ABC1461-25UL
Description
Anti-phospho-c-Myc (Ser347)
Alternate Names
Myc proto-oncogene protein
Class E basic helix-loop-helix protein 39
bHLHe39
Proto-oncogene c-Myc
c-Myc
Transcription factor p64
Background Information
Myc proto-oncogene protein (UniProt: P01106; also known as Class E basic helix-loop-helix protein 39, bHLHe39, Proto-oncogene c-Myc, Transcription factor p64) is encoded by the MYC (also known as BHLHE39) gene (Gene ID: 4609) in human. c-Myc is a transcription factor that binds DNA in a non-specific manner, yet also specifically recognizes the core sequence 5'-CAC[GA]TG-3'. It regulates the expression of multiple genes involved in apoptosis, cell differentiation and cell proliferation. c-Myc is shown to be critically involved in the regulation of several growth promoting signaling pathways and is considered as an immediate early response gene that is downstream of many ligand-membrane receptor complexes. Its expression is reported to be tightly regulated by several transcriptional regulatory motifs within its proximal promoter region. Phosphorylation of c-Myc by serine/threonine kinase PIM2 at serine 329 is reported to lead to its stabilization. Active c-Myc is coupled to the MAX protein via its C-terminal helix-loop-helix leucine zipper (bHLHLZ) domain (aa 413-434) and this heterodimer interacts with a number of other transcription-related proteins. In normal cells its expression and function are regulated by developmental or mitogenic signals. c-Myc mRNA has a very short half-life and in the absence of positive regulatory signals there is a significant reduction in its transcription leading to low c-Myc protein levels that does not have any proliferative drive. However, in tumor cells its levels are increased either via mutations or induction via upstream oncogenic pathways. Serine 347/348 are shown to be phosphorylated by casein kinase II. S347A/S348A reported to be more potent oncogenic mutants compared with wild-type c-Myc. Mutations leading to S347A/S348A are known to enhance transformation of cells compared to wild types. Mutations in c-Myc gene have been linked to B-cell chronic lymphocytic leukemia and Burkitt lymphoma. Over-expression of c-Myc has been reported in about 40% tumors. (Ref.: Wasylishen, AR., et al. (2013). Cancer Res. 73(21); 6504-6515; Miller, DM et al., (2012). Clin. Cancer Res. 18(20); 5546 5553; Lutterbach, B., and Hann, SR (1997). Oncogene. 14(8); 967-975).
References
Product Information
Format
Purified
Presentation
Purified rabbit polyclonal antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
Anti-phospho-c-Myc (Ser347), Cat. No. ABC1461, is a rabbit polyclonal antibody that detects c-Myc phosphorylated on serine 347 and is tested for use in Peptide Inhibition Assay and Western Blotting.
Key Applications
Peptide Inhibition Assay
Western Blotting
Application Notes
Western Blotting Analysis: A 1:500 dilution from a representative lot detected phospho-c-Myc (Ser347) in HEK293T cells transfected with V5-WT-Myc and treated with MG132 (Courtesy of Dr. Linda Penn Lab @ Princess Margaret Cancer center, part of the University Health Network, Toronto).
Peptide Inhibition Assay: Target band detection in lysate from HEK293T cells transfected with V5-WT-Myc and treated with MG132 (10 mM; 4 h) was prevented by preblocking of a representative lot with the immunogen phosphopeptide, but not the control peptide.
Peptide Inhibition Assay: A 1:500 dilution from a representative lot was used with HEK293T cells transfected with V5-WT-Myc and treated with MG132 for peptide block analysis (Courtesy of Dr. Linda Penn Lab @ Princess Margaret Cancer Centre, part of the University Health Network, Toronto).
Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user
Biological Information
Immunogen
KLH-conjugated linear peptide corresponding to 10 amino acids surrounding phosphoserine 347 from the C-terminal half of human c-Myc.
Epitope
C-terminus
Concentration
0.5 mg/mL. Please refer to guidance on suggested starting dilutions and/or titers per application and sample type.
Host
Rabbit
Specificity
This rabbit polyclonal antibody detects c-Myc phosphorylated on serine 347. It targets an epitope within 10 amino acids surrounding phosphoserine 347 from the C-terminal half.
Isotype
IgG
Species Reactivity
Human
Species Reactivity Note
Human. Predicted to react with Non-Human Primates based on 100% sequence homology.
~58 kDa observed; 48.80 kDa calculated. Uncharacterized bands may be observed in some lysate(s).
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Quality Assurance
Evaluated by Western Blotting in HEK293T transfected with V5-WT-Myc and treated with MG132.
Western Blotting Analysis: A 1:500 dilution of this antibody detected c-Myc phosphorylated on serine 347 in lysate from HEK293T cells transfected with V5 tagged-wild-type c-Myc and treated with MG132 (10 µM, 4 h).
Usage Statement
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Storage and Shipping Information
Storage Conditions
Stable for 1 year at +2°C to +8°C from date of receipt.