Rabbit Polyclonal C4orf48 antibody. Suitable for IHC-P, ICC/IF and reacts with Human samples. Cited in 3 publications. Immunogen corresponding to Recombinant Fragment Protein within Human NICOL1 aa 1-100.
View Alternative Names
C4orf48, NICOL1, NELL2-interacting cell ontogeny regulator 1, NELL2-interacting cofactor for lumicrine signaling, NICOL
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-C4orf48 antibody (AB185315)
Immunohistochemical analysis of paraffin-embedded human cerebral cortex tissue labeling C4orf48 in the cytoplasm of neuronal cells with ab185315 at a 1/50 dilution.
Performed heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-C4orf48 antibody (AB185315)
Immunocytochemistry analysis of PC-3 (human prostate adenocarcinoma cell line) whole cells labeling C4orf48 in the cytosol with ab185315 at 2 μg/ml.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-C4orf48 antibody (AB185315)
Immunohistochemical analysis of paraffin-embedded human skin tissue labeling C4orf48 in the cytoplasm of neuronal cells with ab185315 at a 1/50 dilution.
Performed heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Reactivity data
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Supplementary information
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Biological function summary
C4orf48 contributes to cellular processes such as growth and development. Current studies reveal no specific involvement in a larger protein complex suggesting it might function independently or as part of transient molecular interactions. Further investigations are necessary to establish detailed biological roles and interactions of C4orf48.
Pathways
Current data suggests that C4orf48 interacts with cellular pathways influencing transcription and signaling. It seems to have interactions with pathways potentially involving histological modulation though precise partners and downstream effects need clarification. Researchers have suggested potential crosstalk with proteins involved in regulatory networks but no definitive pathway integration has been identified yet.
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Publications (3)
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The Journal of clinical investigation 134: PubMed38625739
2024
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Biological & pharmaceutical bulletin 45:200-206 PubMed35110507
2022
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Nature communications 11:1312 PubMed32161263
2020
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