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Immunofluorescent analysis of MCF-7 cells using CSB-PA001388LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
Immunofluorescent analysis of MCF-7 cells using CSB-PA001388LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
Immunofluorescent analysis of MCF-7 cells using CSB-PA001388LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)

ADRA2A Antibody

CSB-PA001388LA01HU
Cusabio
ApplicationsImmunoFluorescence, ELISA
Product group Antibodies
TargetADRA2A
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Overview

  • Supplier
    Cusabio
  • Product Name
    ADRA2A Antibody
  • Delivery Days Customer
    20
  • Applications
    ImmunoFluorescence, ELISA
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID150
  • Target name
    ADRA2A
  • Target description
    adrenoceptor alpha 2A
  • Target synonyms
    ADRA2; ADRA2R; ADRAR; adrenergic, alpha-2A-, receptor; alpha-2 adrenergic receptor subtype C10; alpha-2A adrenergic receptor; alpha-2A adrenoceptor; alpha-2A adrenoreceptor; ALPHA2AAR; alpha-2AAR subtype C10; alpha-2-adrenergic receptor, platelet type; ZNF32
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP08913
  • Protein Name
    Alpha-2A adrenergic receptor
  • Scientific Description
    Alpha-2 adrenergic receptors mediate the catecholamine-induced inhibition of adenylate cyclase through the action of G proteins. The rank order of potency for agonists of this receptor is oxymetazoline > clonidine > epinephrine > norepinephrine > phenylephrine > dopamine > p-synephrine > p-tyramine > serotonin = p-octopamine. For antagonists, the rank order is yohimbine > phentolamine = mianserine > chlorpromazine = spiperone = prazosin > propanolol > alprenolol = pindolol.
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of alpha 2a Adrenergic Receptor/ADRA2A using anti-alpha 2a Adrenergic Receptor/ADRA2A antibody (A00883-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat pancreas tissue lysates, Lane 2: rat small intestine tissue lysates, Lane 3: mouse pancreas tissue lysates, Lane 4: mouse small intestine tissue lysate. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-alpha 2a Adrenergic Receptor/ADRA2A antigen affinity purified polyclonal antibody (Catalog # A00883-3) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for alpha 2a Adrenergic Receptor/ADRA2A at approximately 55 kDa. The expected band size for alpha 2a Adrenergic Receptor/ADRA2A is at 49 kDa.
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