"APOC1" Related Products

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Native Human ApoC-I

Cat.No.: ApoC-I-3557H
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.
Source: Human plasma
Species: Human
Form: Lyophilized from 10mM NH4HCO3, pH 7.4.
Molecular Mass: 6.6 kDa
Purity: >95% pure by SDS PAGE
Notes: Small volumes of ApoC-I native protein may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice.
Storage: Aliquot and store at -20 deg C. Avoid repeated freeze/thaw cycles.
Warning: This product is for research use only. Not for use in diagnostic or therapeutic procedures.
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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