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This peptide corresponds to 17 amino acid peptide near the amino terminus of human COH1.
PEP-1448 can be used as a blocking peptide with polyclonal antibody PA5-34406.
COH1 (Cohen syndrome protein 1), also known as VPS13B (vacuolar protein sorting-associated protein 13B) or CHS1, belongs to the VPS13 family and may function in vesicle-mediated transport and sorting of proteins within the cell. COH1 is widely expressed and multiple alternatively spliced transcript variants have been observed. Mutations in this gene have been associated with Cohen syndrome. COH1 is a Golgi-localized peripheral membrane protein and plays a critical role in Golgi (re)assembly.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Cohen syndrome protein 1; Intermembrane lipid transfer protein VPS13B; Vacuolar protein sorting-associated protein 13B
Gene Aliases: CHS1; COH1; KIAA0532; VPS13B
UniProt ID: (Human) Q7Z7G8
Entrez Gene ID: (Human) 157680
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