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
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
Tested Application Dilution
ICC/IF1:200 - 1:500
IHC-P1:200 - 1:500
WB1:1000 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
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

GeneID: 335 Human APOA1

Swiss-port # P02647 Human Apolipoprotein A-I

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]