Anti-ATPB Rabbit antibody

Cat.#: 167519

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Product Information

  • Product Name
    Anti-ATPB Rabbit antibody
  • Documents
  • Description
    ATPB Rabbit polyclonal antibody
  • Tested applications
    WB, IHC-P, ICC/IF, IP
  • Species reactivity
    Human, Mouse, Rat
  • Alternative names
    ATP5B; ATPMB; ATPSB; HEL-S-271 antibody
  • Isotype
    Rabbit IgG
  • Preparation
    Antigen: A synthetic peptide of human ATPB
  • Clonality
    Polyclonal
  • Formulation
    Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M Nacl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA.
  • Storage instructions
    Store at -20°C. Stable for 12 months from date of receipt.
  • Applications

    WB: 1/2000-1/10000

    IHC: 1/20-1/100

    ICC/IF: 1/50

    IP: 1/20-1/50

  • Validations

    Immunohistochemistry of ATPB in paraffin-embedded Human tonsil using ATPB Rabbit pAb at dilution 1/20

    Immunohistochemistry of ATPB in paraffin-embedded Human tonsil using ATPB Rabbit pAb at dilution 1/20

    Immunocytochemistry of ATPB(green) in Hela cells using ATPB Rabbit pAb at dilution 1/50, and DAPI(blue)

    Immunocytochemistry of ATPB(green) in Hela cells using ATPB Rabbit pAb at dilution 1/50, and DAPI(blue)

    Western blot detection of ATPB in Jurkat,Hela,COS7,Raji cell lysates using ATPB Rabbit pAb(1:1000 diluted).Predicted band size:57KDa.Observed band size:52KDa.

    Western blot detection of ATPB in Jurkat,Hela,COS7,Raji cell lysates using ATPB Rabbit pAb(1:1000 diluted).Predicted band size:57KDa.Observed band size:52KDa.

  • Background
    Swiss-Prot Acc.P06576.Mitochondrial membrane ATP synthase (F1F0 ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F1 - containing the extramembraneous catalytic core, and F0 - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F1 is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Subunits alpha and beta form the catalytic core in F1. Rotation of the central stalk against the surrounding alpha3beta3 subunits leads to hydrolysis of ATP in three separate catalytic sites on the beta subunits.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"