ApoA-I Polyclonal Antibody
€0.00
In stock
SKU
ELK-ES4169
Catalog Number: ELK-ES4169
Reactivity: Human, Mouse
Applications: WB, IHC-p, ELISA
Information
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Questions? Contact us!
Reactivity: Human, Mouse
Applications: WB, IHC-p, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Background:
apolipoprotein A1(APOA1) Homo sapiens This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The encoded preproprotein is proteolytically processed to generate the mature protein, which promotes cholesterol efflux from tissues to the liver for excretion, and is a cofactor for lecithin cholesterolacyltransferase (LCAT), an enzyme responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein. [provided by RefSeq, Dec 2015],
Alternative Names:
APOA1, Apolipoprotein A-I, Apo-AI, ApoA-I, Apolipoprotein A1
Immunogen: The antiserum was produced against synthesized peptide derived from the Internal region of human APOA1. AA range:81-130
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 31
GeneID: APOA1
Storage: -20°C/1 year
NOTE: For Research Use Only
apolipoprotein A1(APOA1) Homo sapiens This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The encoded preproprotein is proteolytically processed to generate the mature protein, which promotes cholesterol efflux from tissues to the liver for excretion, and is a cofactor for lecithin cholesterolacyltransferase (LCAT), an enzyme responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein. [provided by RefSeq, Dec 2015],
Alternative Names:
APOA1, Apolipoprotein A-I, Apo-AI, ApoA-I, Apolipoprotein A1
Immunogen: The antiserum was produced against synthesized peptide derived from the Internal region of human APOA1. AA range:81-130
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 31
GeneID: APOA1
Storage: -20°C/1 year
NOTE: For Research Use Only
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