ARG67237
anti-Apolipoprotein AI antibody [3A10]
anti-Apolipoprotein AI antibody [3A10] for ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human
Overview
Product Description | Mouse Monoclonal antibody [3A10] recognizes Apolipoprotein AI |
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Tested Reactivity | Hu |
Tested Application | ICC/IF, IHC-P, WB |
Host | Mouse |
Clonality | Monoclonal |
Clone | 3A10 |
Isotype | IgG1 |
Target Name | Apolipoprotein AI |
Antigen Species | Human |
Conjugation | Un-conjugated |
Alternate Names | APOA1; Apolipoprotein A1; Apolipoprotein A-I; Apo-AI; Epididymis Secretory Sperm Binding Protein; AMYLD3; HPALP2; Apo(A); ApoA-I |
Application Instructions
Application Suggestion |
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Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
Form | Liquid |
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Purification | Affinity purified |
Buffer | PBS (pH 7.0), 0.025% ProClin 300 and 20% Glycerol. |
Preservative | 0.025% ProClin 300 |
Stabilizer | 20% Glycerol |
Concentration | 1 mg/ml |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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Gene Symbol | APOA1 |
Gene Full Name | Apolipoprotein A1 |
Background | 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] |
Function | Participates in the reverse transport of cholesterol from tissues to the liver for excretion by promoting cholesterol efflux from tissues and by acting as a cofactor for the lecithin cholesterol acyltransferase (LCAT). As part of the SPAP complex, activates spermatozoa motility. [Uniprot] |
Cellular Localization | Amyloid, HDL, Secreted. [Uniprot] |
Calculated MW | 31 kDa |
PTM | Glycation, Glycoprotein, Lipoprotein, Oxidation, Palmitate, Phosphoprotein. [Uniprot] |