Native Human APOC1

Description :	The protein encoded by this gene is a member of the apolipoprotein C1 family. This gene is expressed primarily in the liver, and it is activated when monocytes differentiate into macrophages. A pseudogene of this gene is located 4 kb downstream in the same orientation, on the same chromosome. This gene is mapped to chromosome 19, where it resides within a apolipoprotein gene cluster. Alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined.
Form :	Lyophilised:Reconstitute with 80ul distilled water.
Purity :	>95% by SDS-PAGE
Storage buffer :	Preservative: NoneConstituents: 10mM Ammonium bicarbonate, pH 7.4
Storage :	Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.
Tag :	Non
Full Length :	Full L.

Gene Name	APOC1 apolipoprotein C-I [ Homo sapiens ]
Official Symbol	APOC1
Synonyms	APOC1; apolipoprotein C-I;
Gene ID	341
mRNA Refseq	NM_001645
Protein Refseq	NP_001636
MIM	107710
Uniprot ID	P02654
Chromosome Location	19q13.2
Pathway	Statin Pathway, organism-specific biosystem;
Function	fatty acid binding; lipase inhibitor activity; phosphatidylcholine binding; phosphatidylcholine-sterol O-acyltransferase activator activity; phospholipase inhibitor activity;