
The data was published in the journal Oncotarget in 2017.PMID: 28460437
c-Myc antibody [9E10]
GTX20032
ApplicationsFlow Cytometry, ImmunoFluorescence, ImmunoPrecipitation, Western Blot, ELISA, ImmunoCytoChemistry
Product group Antibodies
ReactivityHuman
TargetMYC
Overview
- SupplierGeneTex
- Product Namec-Myc antibody [9E10]
- Delivery Days Customer9
- ApplicationsFlow Cytometry, ImmunoFluorescence, ImmunoPrecipitation, Western Blot, ELISA, ImmunoCytoChemistry
- CertificationResearch Use Only
- ClonalityMonoclonal
- ConjugateUnconjugated
- Gene ID4609
- Target nameMYC
- Target descriptionMYC proto-oncogene, bHLH transcription factor
- Target synonymsMRTL, MYCC, bHLHe39, c-Myc, myc proto-oncogene protein, avian myelocytomatosis viral oncogene homolog, class E basic helix-loop-helix protein 39, myc-related translation/localization regulatory factor, proto-oncogene c-Myc, transcription factor p64, v-myc avian myelocytomatosis viral oncogene homolog, v-myc myelocytomatosis viral oncogene homolog
- HostMouse
- IsotypeIgG1
- Protein IDP01106
- Protein NameMyc proto-oncogene protein
- Scientific DescriptionThis gene is a proto-oncogene and encodes a nuclear phosphoprotein that plays a role in cell cycle progression, apoptosis and cellular transformation. The encoded protein forms a heterodimer with the related transcription factor MAX. This complex binds to the E box DNA consensus sequence and regulates the transcription of specific target genes. Amplification of this gene is frequently observed in numerous human cancers. Translocations involving this gene are associated with Burkitt lymphoma and multiple myeloma in human patients. There is evidence to show that translation initiates both from an upstream, in-frame non-AUG (CUG) and a downstream AUG start site, resulting in the production of two isoforms with distinct N-termini. [provided by RefSeq, Aug 2017]
- ReactivityHuman
- Storage Instruction2°C to 8°C
- UNSPSC12352203
References
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- Chang YC, Peng YX, Yu BH, et al. VCP maintains nuclear size by regulating the DNA damage-associated MDC1-p53-autophagy axis in Drosophila. Nat Commun. 2021,12(1):4258. doi: 10.1038/s41467-021-24556-0Read this paper
- Fu SJ, Hu MC, Peng YJ, et al. CUL4-DDB1-CRBN E3 Ubiquitin Ligase Regulates Proteostasis of ClC-2 Chloride Channels: Implication for Aldosteronism and Leukodystrophy. Cells. 2020,9(6). doi: 10.3390/cells9061332Read this paper
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- Thattikota Y, Tollis S, Palou R, et al. Cdc48/VCP Promotes Chromosome Morphogenesis by Releasing Condensin from Self-Entrapment in Chromatin. Mol Cell. 2018,69(4):664-676.e5. doi: 10.1016/j.molcel.2018.01.030Read this paper
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- Shen YR, Wang HY, Kuo YC, et al. SEPT12 phosphorylation results in loss of the septin ring/sperm annulus, defective sperm motility and poor male fertility. PLoS Genet. 2017,13(3):e1006631. doi: 10.1371/journal.pgen.1006631Read this paper


![Indirect ELISA analysis was performed by coating the plate with recombinant Multiple Tags Positive Control ( 6xHis-MBP-DDDDK-V5-HSV-HA-T7-Myc-S) (GTX130342-pro) (57.14-0.89 nM). Coated protein was probed with c-Myc antibody [9E10] (GTX20032) (1 microg/mL). Goat antibody Mouse IgG antibody (HRP) (1:10000) was used to detect the bound primary antibody. Indirect ELISA analysis was performed by coating the plate with recombinant Multiple Tags Positive Control ( 6xHis-MBP-DDDDK-V5-HSV-HA-T7-Myc-S) (GTX130342-pro) (57.14-0.89 nM). Coated protein was probed with c-Myc antibody [9E10] (GTX20032) (1 microg/mL). Goat antibody Mouse IgG antibody (HRP) (1:10000) was used to detect the bound primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX20032/GTX20032_82200350_20240621_ELISA_Indirect_24062501_888.webp)





![ICC/IF analysis of HeLa cells using GTX00684 c-Myc (phospho Ser62) antibody [33A12E10] (Green, Left) or proximity Ligation Analysis with anti-c-Myc pS62 and CIP2A antibodies, association of c-Myc pS62 with CIP2A (Right, red) in nuclei (DAPI, blue).](https://www.genetex.com/upload/website/prouct_img/normal/GTX00684/GTX00684_20191104_ICC-IF_1_w_23053121_552.webp)
![Untreated (-) and treated (+) HepG2 whole cell extracts (30 microg) were separated by 10% SDS-PAGE, and the membrane was blotted with c-Myc (phospho Thr58/Ser62) antibody [SZ02-06] (GTX01137) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX01137/GTX01137_HK1219_20200228_WB_treatment_MG132_w_23053121_696.webp)