M4439
Anti-c-Myc antibody, Mouse monoclonal
clone 9E10, purified from hybridoma cell culture
Synonym(s):
Anti-c-Myc
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About This Item
UNSPSC Code:
12352203
NACRES:
NA.56
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biological source
mouse
Quality Level
conjugate
unconjugated
antibody form
purified from hybridoma cell culture
antibody product type
primary antibodies
clone
9E10, monoclonal
form
buffered aqueous solution
mol wt
62 kDa
species reactivity
human
concentration
~2 mg/mL
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This Item | 33303 | 33300 | 33301 |
|---|---|---|---|
| material white PTFE valve | material white PTFE valve | material white PTFE valve | material white PTFE valve |
| compatibility for use with 20 mm crimp seal | compatibility for use with 20/400 mm thread | compatibility for use with 13/425 mm thread | compatibility for use with 15/425 mm thread |
| packaging pkg of 12 ea | packaging pkg of 12 ea | packaging pkg of 12 ea | packaging pkg of 12 ea |
General description
The mouse Anti-c-MYC monoclonal antibody recognizes an epitope located within a sequence (EQKLISEEDL) of the product of the human oncogene c-myc.
c-Myc (v-myc avian myelocytomatosis viral oncogene homolog) is a transcription factor, which is coded by MYC gene. It was first described as a homolog of an avian retroviral oncogene. It belongs to the family of transcription factors which are characterized by basic region helix-loop-helix/leucine zipper.[1] Along with N-Myc and L-Myc, it forms the MYC proto-oncogene family.[2] It forms a heterodimer with MAX, and this heterodimer binds to the E-boxes/CACGTG sequence motif on DNA.[1] This gene is localized to human chromosome 8q24.[3]
Immunogen
synthetic peptide of the human p62c-Myc protein.
Application
Biochem/physiol Actions
v-myc avian myelocytomatosis viral oncogene homolog belongs to MYC family. When overexpressed these proteins can cause DNA double-stand breaks (DSBs) and genome instability.[12] This transcription factor MYC helps in regulating long noncoding RNAs (lncRNAs) which has been implicated in cancer cell proliferation and tumorigenesis.[13] Its overexpression is also associated with various cancers, and in particular B cell lymphomas. Increased expression of c-MYC has a negative effect on the ability of B cell lymphomas to functionally present Ags/peptides to CD4+ T cells. This protein exerts suppressive effects at several critical checkpoints in Ag presentation.[1] It is associated with Burkitt lymphoma and a group of diffuse large B-cell lymphoma (DLBCL).[14]
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
Preparation Note
Working dilution: 1:5000
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Pricing
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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Željka Škunca et al.
Acta medica Croatica : casopis Hravatske akademije medicinskih znanosti, 68(3), 299-305 (2015-05-29)
Diffuse large B-cell lymphoma (DLBCL) is classified as lymphoma and various entities using the gene expression of proteins are classified into three groups. The aim of this study was to clarify the clinical, biological, immunophenotypic and cytogenetic features of DLBCL
Taewan Kim et al.
Journal of the National Cancer Institute, 107(4), doi:10-doi:10 (2015-02-11)
The functions of long noncoding RNAs (lncRNAs) have been identified in several cancers, but the roles of lncRNAs in colorectal cancer (CRC) are less well understood. The transcription factor MYC is known to regulate lncRNAs and has been implicated in
Susanna Ambrosio et al.
Mutation research, 774, 6-13 (2015-03-17)
Although it is established that when overexpressed, the MYC family proteins can cause DNA double-stand breaks (DSBs) and genome instability, the mechanisms involved remain unclear. MYC induced genetic instability may result from increased DNA damage and/or reduced DNA repair. Here
Mirjana Macvanin et al.
Journal of bacteriology, 194(22), 6046-6055 (2012-09-04)
Some unidentified RNA molecules, together with the nucleoid protein HU, were suggested to be involved in the nucleoid structure of Escherichia coli. HU is a conserved protein known for its role in binding to DNA and maintaining negative supercoils in
Kimberly J Perry et al.
Developmental biology, 374(2), 281-294 (2013-01-01)
Understanding the biology of somatic stem cells in self renewing tissues represents an exciting field of study, especially given the potential to harness these cells for tissue regeneration and repair in treating injury and disease. The mammalian cornea contains a
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