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Figure 1. Western blot analysis of N WASP/WASL using anti-N WASP/WASL antibody (A05438-3). 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 50ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U87 whole cell lysates, Lane 3: human HELA whole cell lysates, Lane 4: human CACO-2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: rat liver tissue lysates, Lane 8: rat C6 whole cell lysates, Lane 9: mouse brain tissue lysayes, Lane 10: mouse lung tissue lysates, Lane 11: mouse liver tissue lysates, Lane 12: mouse Neuro-2a whole cell lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-N WASP/WASL antigen affinity purified polyclonal antibody (Catalog # A05438-3) 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 N WASP/WASL at approximately 70KD. The expected band size for N WASP/WASL is at 70KD.
Figure 1. Western blot analysis of N WASP/WASL using anti-N WASP/WASL antibody (A05438-3). 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 50ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U87 whole cell lysates, Lane 3: human HELA whole cell lysates, Lane 4: human CACO-2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: rat liver tissue lysates, Lane 8: rat C6 whole cell lysates, Lane 9: mouse brain tissue lysayes, Lane 10: mouse lung tissue lysates, Lane 11: mouse liver tissue lysates, Lane 12: mouse Neuro-2a whole cell lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-N WASP/WASL antigen affinity purified polyclonal antibody (Catalog # A05438-3) 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 N WASP/WASL at approximately 70KD. The expected band size for N WASP/WASL is at 70KD.
Figure 1. Western blot analysis of N WASP/WASL using anti-N WASP/WASL antibody (A05438-3). 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 50ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U87 whole cell lysates, Lane 3: human HELA whole cell lysates, Lane 4: human CACO-2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: rat liver tissue lysates, Lane 8: rat C6 whole cell lysates, Lane 9: mouse brain tissue lysayes, Lane 10: mouse lung tissue lysates, Lane 11: mouse liver tissue lysates, Lane 12: mouse Neuro-2a whole cell lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-N WASP/WASL antigen affinity purified polyclonal antibody (Catalog # A05438-3) 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 N WASP/WASL at approximately 70KD. The expected band size for N WASP/WASL is at 70KD.

Anti-N WASP/WASL Antibody Picoband(r)

A05438-3-BIOTIN
Boster Bio
ApplicationsFlow Cytometry, Western Blot, ELISA
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetWASL
100 ug
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Overview

  • Supplier
    Boster Bio
  • Product Name
    Anti-N WASP/WASL Antibody Picoband(r)
  • Delivery Days Customer
    9
  • Applications
    Flow Cytometry, Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    500 ug/ml
  • Conjugate
    Biotin
  • Gene ID8976
  • Target name
    WASL
  • Target description
    WASP like actin nucleation promoting factor
  • Target synonyms
    neural Wiskott-Aldrich syndrome protein; NWASP; N-WASP; WASPB; Wiskott-Aldrich syndrome like
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO00401
  • Protein Name
    Neural Wiskott-Aldrich syndrome protein
  • Scientific Description
    Boster Bio Anti-N WASP/WASL Antibody Picoband® catalog # A05438-3. Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352203