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Figure 1. Western blot analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). 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 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human LNCAP whole cell lysates, Lane 6: human U2OS whole cell lysates, Lane 7: human RT4 whole cell lysates, Lane 8: rat C6 whole cell lysates, Lane 9: rat PC-12 whole cell lysates, Lane 10: mouse NIH/3T3 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-HnRNP H/HNRNPH1 antigen affinity purified polyclonal antibody (Catalog # A07691) 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 HnRNP H/HNRNPH1 at approximately 49 kDa. The expected band size for HnRNP H/HNRNPH1 is at 49 kDa.
Figure 1. Western blot analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). 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 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human LNCAP whole cell lysates, Lane 6: human U2OS whole cell lysates, Lane 7: human RT4 whole cell lysates, Lane 8: rat C6 whole cell lysates, Lane 9: rat PC-12 whole cell lysates, Lane 10: mouse NIH/3T3 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-HnRNP H/HNRNPH1 antigen affinity purified polyclonal antibody (Catalog # A07691) 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 HnRNP H/HNRNPH1 at approximately 49 kDa. The expected band size for HnRNP H/HNRNPH1 is at 49 kDa.
Figure 1. Western blot analysis of HnRNP H/HNRNPH1 using anti-HnRNP H/HNRNPH1 antibody (A07691). 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 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human LNCAP whole cell lysates, Lane 6: human U2OS whole cell lysates, Lane 7: human RT4 whole cell lysates, Lane 8: rat C6 whole cell lysates, Lane 9: rat PC-12 whole cell lysates, Lane 10: mouse NIH/3T3 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-HnRNP H/HNRNPH1 antigen affinity purified polyclonal antibody (Catalog # A07691) 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 HnRNP H/HNRNPH1 at approximately 49 kDa. The expected band size for HnRNP H/HNRNPH1 is at 49 kDa.

Anti-HnRNP H/HNRNPH1 Antibody Picoband(r)

A07691-CARRIER-FREE
Boster Bio
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
TargetHNRNPH1
100 ug
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Overview

  • Supplier
    Boster Bio
  • Product Name
    Anti-HnRNP H/HNRNPH1 Antibody Picoband(r)
  • Delivery Days Customer
    9
  • Application Supplier Note
    Tested Species: In-house tested species with positive results. Other applications have not been tested. Optimal dilutions should be determined by end users.
  • Applications
    Flow Cytometry, ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    500 ug/ml
  • Gene ID3187
  • Target name
    HNRNPH1
  • Target description
    heterogeneous nuclear ribonucleoprotein H1
  • Target synonyms
    epididymis secretory sperm binding protein; heterogeneous nuclear ribonucleoprotein H; heterogeneous nuclear ribonucleoprotein H1 (H); hnRNPH; HNRPH; HNRPH1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP31943
  • Protein Name
    Heterogeneous nuclear ribonucleoprotein H
  • Scientific Description
    Boster Bio Anti-HnRNP H/HNRNPH1 Antibody Picoband® catalog # A07691. Tested in Flow Cytometry, IF, IHC, ICC, 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.
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352203

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