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Recombinant Human APOC1 cell lysate

Cat.No.: APOC1-97HCL
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.
Species: Human
Size: 100 ul
Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications: Western Blot;
Gene Name: APOC1 apolipoprotein C-I [ Homo sapiens ]
Official Symbol: APOC1
Synonyms: APOC1; apolipoprotein C-I; apo-CIB; apoC-IB; apolipoprotein C1;
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;

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