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SMCR7 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

SMCR7 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2732246
  • Antigène Voir toutes SMCR7 Protéines
    SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 1
    Origine
    • 3
    • 2
    • 1
    Humain
    Source
    • 4
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette SMCR7 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human SMCR7 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product SMCR7 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    SMCR7 (Smith-Magenis Syndrome Chromosome Region, Candidate 7 (SMCR7))
    Autre désignation
    Smcr7 (SMCR7 Produits)
    Synonymes
    AI482195 Protein, Gm11 Protein, MID49 Protein, mid49 Protein, Smcr7 Protein, RGD1560728 Protein, SMCR7 Protein, im:7149098 Protein, smcr7 Protein, smcr7b Protein, zgc:152920 Protein, mitochondrial elongation factor 2 Protein, mitochondrial elongation factor 2 S homeolog Protein, Mief2 Protein, MIEF2 Protein, mief2.S Protein, mief2 Protein
    Sujet
    This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms.
    Poids moléculaire
    49.1 kDa
    NCBI Accession
    NP_631901
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