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Apolipoprotein A1 antibody (HRP)

Cat. No. GTX40784

Host

 Goat

Clonality

 Polyclonal

Isotype

 IgG

Application

 WB, ELISA, Immunoassay

Reactivity

 Human
Package
100 μl ($399)
See all Apolipoprotein A1 products

APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.
Application Recommended Dilution
WB Assay dependent
ELISA 1:200-1:8,000
Immunoassay Assay dependent
Not tested in other applications.

Calculated MW

31 kDa. ( Note )

Product Note

Specific binding to Apo A-I.

PROPERTIES

Form

Liquid

Buffer

50mM PBS, 100mM NaCl, 1% BSA

Preservative

0.01% Thimerosal

Storage

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

Concentration

1 mg/ml (Please refer to the vial label for the specific concentration.)

Antigen Species

Human

Immunogen

Purified human Apo AI

Purification

Purified by Affinity chromatography

Conjugation

Horseradish peroxidase(HRP)

Note

For laboratory research use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.

Purchasers shall not, and agree not to enable third parties to, analyze, copy, reverse engineer or otherwise attempt to determine the structure or sequence of the product.

TARGET

Synonyms

apolipoprotein A1 , apo(a)

Cellular Localization

Secreted

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]

Database

Research Area

REFERENCE

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REVIEW

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SDS
PBS.pdf
Thimerosal.pdf
Package List Price ($)
$ 399