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Brp44L Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-70532

  • Amount:

    100ul

  • Molecular Weight:

    12347Da

  • Applications:

    WB;IHC-p;IF/ICC;ELISA

  • Reactivity:

    Human;Mouse;Rat

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human BRP44L. AA range:11-60

  • Source:

    Polyclonal, Rabbit,IgG

  • Immunofluorescence analysis of Hela cell. 1,Brp44L Polyclonal Antibody(green) was diluted at 1:200(4° overnight). (red) was diluted at 1:200(4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 Catalog:RS3211 was diluted at 1:1000(room temperature, 50min). Goat Anti Mouse Alexa Fluor 594 Catalog:RS3608 was diluted at 1:1000(room temperature, 50min).

  • Gene Name:

    MPC1

  • Dilution:

    Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000. Not yet tested in other applications.

  • Protein Name:

    Mitochondrial pyruvate carrier 1

  • Human Gene Id:

    51660

  • Human Swiss Prot No:

    Q9Y5U8

  • Mouse Gene Id:

    55951

  • Mouse Swiss Prot No:

    P63030

  • Rat Gene Id:

    171087

  • Rat Swiss Prot No:

    P63031

  • Specificity:

    Brp44L Polyclonal Antibody detects endogenous levels of Brp44L protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    MPC1; BRP44L; CGI-129; HSPC040; PNAS-115; Mitochondrial pyruvate carrier 1; Brain protein 44-like protein

  • Observed Band(KD):

    12

  • Background:

    The protein encoded by this gene is part of an MPC1/MPC2 heterodimer that is responsible for transporting pyruvate into mitochondria. The encoded protein is found in the inner mitochondrial membrane. Defects in this gene are a cause of mitochondrial pyruvate carrier deficiency. Several transcript variants, some protein coding and one non-protein coding, have been found for this gene. [provided by RefSeq, Aug 2012],

  • Function:

    similarity:Belongs to the UPF0041 (0-44) family.,

  • Subcellular Location:

    Mitochondrion inner membrane ; Multi-pass membrane protein .

  • Expression:

    Placenta,Promyelocytic leukemia,Skeletal muscle,Umbilical cord blood,

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Catalog Number

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