ApoA-I rabbit pAb

ApoA-I rabbit pAb

AO-06-ES4169-50

ApoA-I rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES4169
Product nameApoA-I rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;IHC;IF;ELISA
Other nameAPOA1; Apolipoprotein A-I; Apo-AI; ApoA-I; Apolipoprotein A1
Size50μL
Unit price ($)148
Human gene ID335
Human Swiss-ProtP02647
SourceRabbit
IsotypeIgG
TargetApoA-I
Fields>>PPAR signaling pathway;>>Fat digestion and absorption;>>Vitamin digestion and absorption;>>Cholesterol metabolism;>>African trypanosomiasis;>>Lipid and atherosclerosis
Gene nameAPOA1
Protein nameApolipoprotein A-I
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID11806
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ00623
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from the Internal region of human APOA1. AA range:81-130
SpecificityApoA-I Polyclonal Antibody detects endogenous levels of ApoA-I protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1/100-1/300. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)31kD
BackgroundThis 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],
Functiondisease:Defects in APOA1 are a cause of amyloidosis type 8 (AMYL8) [MIM:105200]; also known as systemic non-neuropathic amyloidosis or Ostertag-type amyloidosis. AMYL8 is a hereditary generalized amyloidosis due to deposition of apolipoprotein A1, fibrinogen and lysozyme amyloids. Viscera are particularly affected. There is no involvement of the nervous system. Clinical features include renal amyloidosis resulting in nephrotic syndrome, arterial hypertension, hepatosplenomegaly, cholestasis, petechial skin rash.,disease:Defects in APOA1 are a cause of high density lipoprotein deficiency type 2 (HDLD2) [MIM:604091]; also known as familial hypoalphalipoproteinemia (FHA). Inheritance is autosomal dominant.,disease:Defects in APOA1 are a cause of the low HDL levels observed in high density lipoprotein deficiency type 1 (HDLD1) [MIM:205400]; also known as analphalipoproteinemia or Tangier dis
Subcellular locationSecreted.
ExpressionMajor protein of plasma HDL, also found in chylomicrons. Synthesized in the liver and small intestine. The oxidized form at Met-110 and Met-136 is increased in individuals with increased risk for coronary artery disease, such as in carrier of the eNOSa/b genotype and exposure to cigarette smoking. It is also present in increased levels in aortic lesions relative to native ApoA-I and increased levels are seen with increasing severity of disease.

Additional Images

Image 1
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Western Blot analysis of K562 cells using ApoA-I Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
Image 3
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Immunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
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Immunohistochemical analysis of paraffin-embedded human-lung, antibody was diluted at 1:100
: AO-06-ES4169-50
: 10 Produits
Hurry! only 10 items left in stock.

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