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ProductsBack/Goat anti-ARP2/3 subunit 1B

Goat anti-ARP2/3 subunit 1B

EB05435
Everest Biotech
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry
Product group Antibodies
TargetARPC1B
100 ug
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Overview

  • Supplier
    Everest Biotech
  • Product Name
    Goat anti-ARP2/3 subunit 1B Antibody
  • Delivery Days Customer
    5
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry
  • Applications Supplier
    Pep-ELISA, WB, IHC
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5 mg/ml
  • Gene ID10095
  • Target name
    ARPC1B
  • Target description
    actin related protein 2/3 complex subunit 1B
  • Target synonyms
    actin related protein 2/3 complex, subunit 1B, 41kDa; actin-related protein 2/3 complex subunit 1B; ARC41; arp2/3 complex 41 kDa subunit; ARP2/3 protein complex subunit p41; IMD71; p40-ARC; p41-ARC; PLTEID
  • Host
    Goat
  • Scientific Description
    RefSeq number(s): NP_005711.1. Purification: Antigen affinity purified. Names and symbols: ARPC1B; actin related protein 2/3 complex, subunit 1B, 41kDa; ARC41; p40-ARC; p41-ARC; ARP2/3 protein complex subunit p41; actin related protein 2/3 complex, subunit 1A (41 kD); OTTHUMP00000206020
  • Reactivity Supplier
    Human, Mouse, Rat, Dog, Pig, Cow
  • Storage Instruction
    -20°C
  • UNSPSC
    12352203

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Figure 1. Flow Cytometry analysis of CACO-2 cells using anti-ARPC1B antibody (A07192-2). Overlay histogram showing CACO-2 cells stained with A07192-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARPC1B Antibody (A07192-2,1microg/1x106 cells) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10microg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1microg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
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