Bio-Connect
Western blot analysis of Cyclin A1/A2 expression in HeLa cell lysate (M00700). 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. 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-CCNA2 monoclonal antibody (Catalog # M00700) 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 1:10000 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 CCNA2
Western blot analysis of Cyclin A1/A2 expression in HeLa cell lysate (M00700). 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. 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-CCNA2 monoclonal antibody (Catalog # M00700) 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 1:10000 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 CCNA2
Western blot analysis of Cyclin A1/A2 expression in HeLa cell lysate (M00700). 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. 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-CCNA2 monoclonal antibody (Catalog # M00700) 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 1:10000 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 CCNA2

Anti-Cyclin A1/A2 Rabbit Monoclonal Antibody

Research Use Only
M00700
Boster Bio
ApplicationsImmunoPrecipitation, Western Blot, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman
TargetCCNA2
Price on request
100 ul
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    Boster Bio
  • Product Name
    Anti-Cyclin A1/A2 Rabbit Monoclonal Antibody
  • Delivery Days Customer
    9
  • Applications
    ImmunoPrecipitation, Western Blot, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    HOD-3
  • Formulation
    Liquid
  • Gene ID890
  • Target name
    CCNA2
  • Target description
    cyclin A2
  • Target synonyms
    CCN1; CCNA; cyclin-A; cyclin-A2
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP20248
  • Protein Name
    Cyclin-A2
  • Scientific Description
    Boster Bio Anti-Cyclin A1/A2 Rabbit Monoclonal Antibody catalog # M00700. Tested in WB, IHC, IP applications. This antibody reacts with Human.
  • Reactivity
    Human
  • Storage Instruction
    -20°C
  • UNSPSC
    12352203

References

  • 15-Lipoxygenase-2/15(S)-hydroxyeicosatetraenoic acid regulates cell proliferation and metastasis via the STAT3 pathway in lung adenocarcinoma. Yang L et al., 2018 Sep, Prostaglandins Other Lipid Mediat
    Read more
  • BST2 promotes cell proliferation, migration and induces NF-kappaB activation in gastric cancer. Liu W et al., 2018 Jul, Biotechnol Lett
    Read more