AB740
Anti-Apolipoprotein A-I Antibody
serum, Chemicon®
Synonym(s):
ApoAI
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About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
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
Specificity
Human apolipoprotein A-I. Monospecific by IEP.
Application
This Anti-Apolipoprotein A-I Antibody is validated for use in WB for the detection of Apolipoprotein A-I.
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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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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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)
Makoto Kurano et al.
PloS one, 12(5), e0177543-e0177543 (2017-05-12)
Sphingosine 1-phosphate (S1P) is a bioactive lipid mediator that is thought to be involved in various diseases. Although the main source of S1P in the plasma is erythrocytes, how S1P is exported from erythrocytes has not been elucidated. When we
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
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
Joseph Verdi et al.
Methods in molecular biology (Clifton, N.J.), 2116, 463-483 (2020-03-30)
Interest in trypanosome lytic factors (TLFs) and apolipoprotein L1, the ion channel-forming protein component of TLFs, has increased tenfold since 2010. This is due to the association of African variants of APOL1 with kidney disease such that interest has reached
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