APOC1 Rabbit pAb
Sizes: 50μL, 100μL
Catalogue Numbers: ES18289-50, ES18289-100
Citations, Manuals and MSDS Available upon request.
Background: This gene encodes a member of the apolipoprotein C1 family. This gene is expressed primarily in the liver, and it is activated when monocytes differentiate into macrophages. The encoded protein plays a central role in high density lipoprotein (HDL) and very low density lipoprotein (VLDL) metabolism. This protein has also been shown to inhibit cholesteryl ester transfer protein in plasma. 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. Alternative splicing and the use of alternative promoters results in multiple transcript variants. [provided by RefSeq, Sep 2016],
Alternate Name: Apolipoprotein C-I (Apo-CIB; ApoC-IB; Apolipoprotein C1) [Cleaved into: Truncated apolipoprotein C-I (Apo-CIB'; ApoC-IB')]
Source: Rabbit
Applications: IHC; ELISA
Dilution: IHC-p 1:50-200, ELISA (peptide)1:5000-20000
Reactivity: Human; Rat; Mouse;
Immunogen: Synthesized peptide derived from human APOC1 AA range: 1-50
Storage and Stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Human Gene ID: 341
Human SWISS Prot NO: P02654
Subcellular Location: Secreted
Research Use Only