Mouse Monoclonal C-Myc/MYC antibody - conjugated to APC. Suitable for Flow Cyt (Intra) and reacts with Tag samples.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: PBS, 1% BSA
Flow Cyt (Intra) | |
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Tag | Tested |
Species | Dilution info | Notes |
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Species Tag | Dilution info 1/500 | Notes The cellular localisation of this product has been verified in ICC/IF. |
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Transcription factor that binds DNA in a non-specific manner, yet also specifically recognizes the core sequence 5'-CAC[GA]TG-3' (PubMed:24940000, PubMed:25956029). Activates the transcription of growth-related genes (PubMed:24940000, PubMed:25956029). Binds to the VEGFA promoter, promoting VEGFA production and subsequent sprouting angiogenesis (PubMed:24940000, PubMed:25956029). Regulator of somatic reprogramming, controls self-renewal of embryonic stem cells (By similarity). Functions with TAF6L to activate target gene expression through RNA polymerase II pause release (By similarity). Positively regulates transcription of HNRNPA1, HNRNPA2 and PTBP1 which in turn regulate splicing of pyruvate kinase PKM by binding repressively to sequences flanking PKM exon 9, inhibiting exon 9 inclusion and resulting in exon 10 inclusion and production of the PKM M2 isoform (PubMed:20010808).
BHLHE39, MYC, Myc proto-oncogene protein, Class E basic helix-loop-helix protein 39, Proto-oncogene c-Myc, Transcription factor p64, bHLHe39
Mouse Monoclonal C-Myc/MYC antibody - conjugated to APC. Suitable for Flow Cyt (Intra) and reacts with Tag samples.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: PBS, 1% BSA
This antibody is specific for Myc tagged proteins. The Myc tag epitope (EQKLISEEDL) is located at the dimerization site of c-myc and therefore this antibody does not perform well at recognizing endogenous c-myc. A publication by Baker AM et al. 2016 (PMID: 26826706 DOI: 10.1111/his.12939) shows the IHC staining generated by the 9E10 clone does not correlate with c-myc mRNA expression.
The Myc tag often referred to as the c-Myc or 9E11 is a synthetic peptide label widely used to facilitate protein purification and detection. It's a short sequence of amino acids with an approximate mass not exceeding 1.2 kDa. Researchers commonly use it because of its easy detection through antibodies like anti-Myc or anti-Myc HRP. This tag is usually fused to proteins of interest in various expression systems including bacterial yeast and mammalian cells.
The Myc tag plays no direct role in cellular processes but enables the study of tagged proteins in complex biological environments. It doesn’t interfere with the function of the protein it tags and is part of no native cellular complex. Instead it acts as a versatile tool for researchers to monitor protein expression levels subcellular localization and interactions. The Myc tag size facilitates easy integration into experimental designs making it compatible with a wide range of applications.
The Myc tag helps map the role of the proteins it is attached to in significant cellular pathways. While the tag itself does not engage in pathways it assists in understanding protein interactions and cellular signaling mechanisms like the MAPK/ERK pathway or the PI3K/Akt pathway. By monitoring tagged proteins scientists can investigate how they interact with other pathway components enabling insights into cellular function and regulation.
The Myc tag aids research into conditions such as cancer and neurodegenerative diseases. The tag itself isn’t linked to any diseases; however it is often used to study proteins involved in these disorders like those in the Myc-oncoprotein family. Researchers use it to examine over-expression or mutation of target proteins connected to disease mechanisms enabling the development of therapeutic approaches and understanding pathogenic processes.
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We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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Flow cytometry analysis of HEK-293T (human embryonic kidney) transfected with Myc-tagged TMEM119 expression vector labelling Myc-tag with ab223896 at 1/500 dilution (right) compared with Mouse IgG1 (monoclonal) Allophycocyanin (left). Cells were surface-stained with TMEM119 antibody (Anti-TMEM119 antibody [106-6] - Microglial marker ab210405), then fixed with 2% PFA for 10 minutes and permeabilised with 0.1% Tween-20 for 30 minutes. Next, they were stained with Allophycocyanin conjugated Myc-tag antibody (ab223896) and Alexa Fluor® 488 conjugated anti-Rabbit secondary antibody (for TMEM119). Only TMEM119 (+) population showed Myc-tag positive staining.
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