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- rabbit polyclonal IgG, 200 µg/ml
- epitope mapping at the N-terminus of QM of human origin
- recommended for detection of QM of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, canine, bovine and porcine
- blocking peptide, sc-799 P
- TransCruz reagent for Gel Supershift and ChIP applications, sc-799 X, 200 µg/0.1 ml
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Ordering InformationProduct Citations
Recommended Support Products:
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| Species |
Gene Name |
Gene ID |
Chromosome Location |
Isoform (mRNA) Accession # |
Protein Accession # |
OMIM™ Number |
| Human |
RPL10L |
140801 |
14q21.3 |
NM_080746 |
Q96L21
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n/a |
| Mouse |
Rpl10 |
110954 |
X A7.3 |
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Q6ZWV3
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N/A |
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QM Background Information The c-Jun protein is a major component of the transcription factor AP-1 (1,2), originally shown to mediate phorbol ester tumor promoter (TPA)-induced expression of responsive genes through the TPA-response element (TRE) (1,2). The Jun proteins form homo- and heterodimers which bind the TRE, while Fos proteins are active only as heterodimers with any of the Jun proteins (3,4). Fos/Jun heterodimers have a much higher affinity for the TRE than Jun homodimers. A distant member of the MAP kinase family, designated c-Jun NH2-terminal kinase (JNK1) functions to regulate c-Jun by phosphorylation at the amino terminal serine regulatory sites, Ser-63 and Ser-73 (5,6). QM has been described as a transcription factor that can function to bind DNA directly or alternatively can interact with c-Jun to inhibit transactivation of AP-1 promoter driven reporter vectors by Jun-Jun homodimers. QM is highly conserved throughout eukaryotic evolution and is apparently a member of a multi-gene family (7).
| QM (N-17) Product Citations |
See how others have used QM (N-17): sc-799 antibody and or QM (N-17) antibody conjugates.
4 total citations Loading citations.
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QM (N-17)
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QM (N-17): sc-799. Western blot analysis of QM expression in HeLa whole cell lysate.
QM (N-17): sc-799. Western blot analysis of QM expression in mouse testis tissue extract.
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