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Immunogen sequence: LIRKYFCSRI QQQAETTSEE LGAVTVKASY RASEQKLRVE LLSASSLLPL DSNGSSDPFV QLTLEPRHEF PELAARETQK HKKDLHPLFD ETFEFLVPAE PCRKAGACLL LTVLDYDTLG ADDLEGEAFL PLREVPGLSG SEEPGEVPQT RLPLTYPAPN GDPILQLLEG RKGDREAQVF VRLRRHRAKQ ASQHALRPAP; Positive Samples: A549, HeLa, HepG2, Mouse lung; Cellular Location: Cytoplasm, Late endosome, Lysosome, Membrane, Peripheral membrane protein, Recycling endosome
This gene encodes a protein that is a member of the UNC13 family, containing similar domain structure as other family members but lacking an N-terminal phorbol ester-binding C1 domain present in other Munc13 proteins. The protein appears to play a role in vesicle maturation during exocytosis and is involved in regulation of cytolytic granules secretion. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis type 3, a genetically heterogeneous, rare autosomal recessive disorder.
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仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: likely ortholog of H. sapiens unc-13 homolog D (UNC13D); munc 13-4; Munc13-4; Protein unc-13 homolog D
基因别名: 2610108D09Rik; FHL3; HLH3; HPLH3; Jinx; mFLJ00067; Munc13-4; UNC13D
UniProt ID: (Human) Q70J99, (Mouse) B2RUP2
Entrez Gene ID: (Human) 201294, (Mouse) 70450