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Western blot All lanes: ATP6V1B2 antibody at 5microg/ml + Hela whole cell lysate Secondary Goat polyclonal to rabbit IgG at 1/10000 dilution Predicted band size: 57 kDa Observed band size: 57 kDa
Western blot All lanes: ATP6V1B2 antibody at 5microg/ml + Hela whole cell lysate Secondary Goat polyclonal to rabbit IgG at 1/10000 dilution Predicted band size: 57 kDa Observed band size: 57 kDa
Western blot All lanes: ATP6V1B2 antibody at 5microg/ml + Hela whole cell lysate Secondary Goat polyclonal to rabbit IgG at 1/10000 dilution Predicted band size: 57 kDa Observed band size: 57 kDa

ATP6V1B2 Antibody

CSB-PA002398ESR1HU
Cusabio
ApplicationsWestern Blot, ELISA
Product group Antibodies
ReactivityHuman
TargetATP6V1B2
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Overview

  • Supplier
    Cusabio
  • Product Name
    ATP6V1B2 Antibody
  • Delivery Days Customer
    20
  • Applications
    Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID526
  • Target name
    ATP6V1B2
  • Target description
    ATPase H+ transporting V1 subunit B2
  • Target synonyms
    ATP6B1B2; ATP6B2; ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2; DOOD; endomembrane proton pump 58 kDa subunit; H+ transporting two-sector ATPase; HO57; testicular secretory protein Li 65; vacuolar H+-ATPase 56,000 subunit; vacuolar proton pump subunit B 2; VATB; V-ATPase B2 subunit; V-ATPase subunit B 2; Vma2; VPP3; V-type proton ATPase subunit B, brain isoform; ZLS2
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP21281
  • Protein Name
    V-type proton ATPase subunit B, brain isoform
  • Scientific Description
    Non-catalytic subunit of the peripheral V1 complex of vacuolar ATPase. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells.
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    41116161

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Figure 1. Western blot analysis of ATP6V1B2 using anti-ATP6V1B2 antibody (A04927-1). 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: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat H9C2(2-1) whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse C2C12 whole cell lysates. 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-ATP6V1B2 antigen affinity purified polyclonal antibody (Catalog # A04927-1) at 0.25 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 ATP6V1B2 at approximately 57 kDa. The expected band size for ATP6V1B2 is at 57 kDa.
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