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PEVR2 (AA 235-284) antibody

This Rabbit Polyclonal antibody specifically detects PEVR2 in IF, WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN1535982
$341.00
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Quick Overview for PEVR2 (AA 235-284) antibody (ABIN1535982)

Target

PEVR2

Reactivity

Human, Mouse, Rat

Host

  • 2
Rabbit

Clonality

  • 2
Polyclonal

Conjugate

  • 2
Un-conjugated

Application

  • 2
  • 2
  • 1
  • 1
Immunofluorescence (IF), Western Blotting (WB), ELISA
  • Binding Specificity

    AA 235-284

    Purpose

    GPR172B Antibody

    Specificity

    GPR172B Polyclonal Antibody detects endogenous levels of GPR172B protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Purity

    > 95 %

    Immunogen

    The antiserum was produced against synthesized peptide derived from human PEVR2. AA range:235-284

    Isotype

    IgG
  • Application Notes

    WB 1:500 - 1:2000. IF 1:200 - 1:1000. ELISA: 1:10000. Not yet tested in other applications.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C/1 year

    Expiry Date

    12 months
  • Target

    PEVR2

    Background

    Synonyms: SLC52A1, GPR172B, PAR2, RFT1, Solute carrier family 52, riboflavin transporter, member 1, Porcine endogenous retrovirus A receptor 2, PERV-A receptor 2, Protein GPR172B, Riboflavin transporter 1, hRFT1

    Background: Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents.This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013],

    Gene Name: SLC52A1

    Protein Name: Solute carrier family 52 riboflavin transporter member 1

    Molecular Weight

    46 kDa

    Gene ID

    55065

    OMIM

    607883

    UniProt

    Q9NWF4
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