Mouse Anti-P4HB Recombinant Antibody (6-9H6) (CBMAB-P0616-YC)

Basic Information
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Cellular response to interleukin-7IEA:Ensembl
Interleukin-12-mediated signaling pathwayTAS:Reactome
Interleukin-23-mediated signaling pathwayTAS:Reactome
Peptidyl-proline hydroxylation to 4-hydroxy-L-prolineManual Assertion Based On ExperimentIDA:MGI
Positive regulation of cell adhesionManual Assertion Based On ExperimentIMP:ARUK-UCL
Positive regulation of substrate adhesion-dependent cell spreadingManual Assertion Based On ExperimentIMP:ARUK-UCL
Positive regulation of viral entry into host cellManual Assertion Based On ExperimentIMP:UniProtKB
Protein foldingManual Assertion Based On ExperimentIBA:GO_Central
Protein folding in endoplasmic reticulumManual Assertion Based On ExperimentIDA:FlyBase
Regulation of oxidative stress-induced intrinsic apoptotic signaling pathwayManual Assertion Based On ExperimentIMP:BHF-UCL
Response to endoplasmic reticulum stressManual Assertion Based On ExperimentIMP:BHF-UCL
Endoplasmic reticulum lumen
Melanosome
Cell membrane
Highly abundant. In some cell types, seems to be also secreted or associated with the plasma membrane, where it undergoes constant shedding and replacement from intracellular sources (Probable). Localizes near CD4-enriched regions on lymphoid cell surfaces (PubMed:11181151).
Identified by mass spectrometry in melanosome fractions from stage I to stage IV (PubMed:10636893).
Colocalizes with MTTP in the endoplasmic reticulum (PubMed:23475612).
A form of Cole-Carpenter syndrome, a disorder characterized by features of osteogenesis imperfecta such as bone deformities and severe bone fragility with frequent fractures, in association with craniosynostosis, ocular proptosis, hydrocephalus, growth failure and distinctive facial features. Craniofacial findings include marked frontal bossing, midface hypoplasia, and micrognathia. Despite the craniosynostosis and hydrocephalus, intellectual development is normal. CLCRP1 inheritance is autosomal dominant.
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols
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Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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