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Merck

AB740

Anti-Apolipoprotein A-I Antibody

serum, Chemicon®

Synonym(s):

ApoAI

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
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biological source

goat

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

species reactivity

human

manufacturer/tradename

Chemicon®

technique(s)

western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Application

This Anti-Apolipoprotein A-I Antibody is validated for use in WB for the detection of Apolipoprotein A-I.

Biochem/physiol Actions

Human apolipoprotein A-I. Monospecific by IEP.

Physical form

Goat serum defibrinated, delipidized and adsorbed by solid phase chromatography as required. Liquid in 0.05M Tris-HCl, pH 7.5, 0.5M NaCl with 0.1% sodium azide.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany


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Storage Class

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Proteomic analysis of plasma-purified VLDL, LDL, and HDL fractions from atherosclerotic patients undergoing carotid endarterectomy: identification of serum amyloid A as a potential marker.
Lepedda, AJ; Nieddu, G; Zinellu, E; De Muro, P; Piredda, F; Guarino, A; Spirito, R; Carta et al.
Oxidative Medicine and Cellular Longevity null
Ronald W Clark et al.
Journal of lipid research, 47(3), 537-552 (2005-12-06)
We have identified a series of potent cholesteryl ester transfer protein (CETP) inhibitors, one member of which, torcetrapib, is undergoing phase 3 clinical trials. In this report, we demonstrate that these inhibitors bind specifically to CETP with 1:1 stoichiometry and
Antonio Junior Lepedda et al.
Journal of circulating biomarkers, 8, 1849454419875912-1849454419875912 (2019-10-08)
Myasthenia gravis (MG) is an autoimmune disease leading to varying degrees of skeletal muscle weakness. It is caused by specific antibodies directed against definite components in the postsynaptic membrane at the neuromuscular junction (NMJ), such as the acetylcholine receptor (AChR)