GPR172A rabbit pAb

GPR172A rabbit pAb

AO-06-ES7582-100

GPR172A rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES7582
Product nameGPR172A rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;IF;ELISA
Other nameSLC52A2; GPR172A; PAR1; RFT3; Solute carrier family 52; riboflavin transporter, member 2; Porcine endogenous retrovirus A receptor 1; PERV-A receptor 1; Protein GPR172A; Riboflavin transporter 3; hRFT3
Size100μL
Unit price ($)248
Human gene ID79581
Human Swiss-ProtQ9HAB3
SourceRabbit
IsotypeIgG
TargetGPR172A
Fields
Gene nameSLC52A2
Protein nameSolute carrier family 52 riboflavin transporter member 2
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtQ9D8F3
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 human PEVR1. AA range:43-92
SpecificityGPR172A Polyclonal Antibody detects endogenous levels of GPR172A protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000. 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)46kD
BackgroundThis gene encodes a membrane protein which belongs to the riboflavin transporter family. In humans, riboflavin must be obtained by intestinal absorption because it cannot be synthesized by the body. The water-soluble vitamin riboflavin is processed to the coenzymes flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) which then act as intermediaries in many cellular metabolic reactions. Paralogous members of the riboflavin transporter gene family are located on chromosomes 17 and 20. Unlike other members of this family, this gene has higher expression in brain tissue than small intestine. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. Mutations in this gene have been associated with Brown-Vialetto-Van Laere syndrome 2 - an autosomal recessive progressive neurologic disorder characterized by deafness, bulbar dysfunctio
Functionfunction:Acts as cell surface receptor for porcine endogenous retrovirus (PERV-A).,similarity:Belongs to the PERVR family.,tissue specificity:Detected in a wide variety of tissues. High expression in testis.,
Subcellular locationCell membrane ; Multi-pass membrane protein .
ExpressionHighly expressed in brain, fetal brain and salivary gland. Weakly expressed in other tissues.

Additional Images

Image 1
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Western Blot analysis of A549 cells using GPR172A Polyclonal Antibody
Image 2
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Immunofluorescence analysis of MCF7 cells, using PEVR1 Antibody. The picture on the right is blocked with the synthesized peptide.
Image 3
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Western blot analysis of lysates from A549 cells, using PEVR1 Antibody. The lane on the right is blocked with the synthesized peptide.
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Western blot analysis of the lysates from HepG2 cells using PEVR1 antibody.
: AO-06-ES7582-100
: 10 Produits
Hurry! only 10 items left in stock.

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