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BSND Protein (AA 221-320) (GST tag)

BSND Origine: Humain Hôte: Wheat germ Recombinant ELISA, WB, AA, AP
N° du produit ABIN1346907
  • Antigène Voir toutes BSND Protéines
    BSND (Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 221-320
    Origine
    • 3
    • 2
    Humain
    Source
    • 2
    • 2
    • 1
    Wheat germ
    Purification/Conjugué
    Cette BSND protéine est marqué à la GST tag.
    Application
    ELISA, Western Blotting (WB), Antibody Array (AA), Affinity Purification (AP)
    Fonction
    BSND (Human) Recombinant Protein (Q01)
    Séquence
    ACSPQQEPQG CRCPLDRFQD FALIDAPTLE DEPQEGQQWE IALPNNWQRY PRTKVEEKEA SDTGGEEPEK EEEDLYYGLP DGAGDLLPDK ELGFEPDTQG
    Attributs du produit
    Human BSND partial ORF ( NP_476517.1, 221 a.a. - 320 a.a.) recombinant protein with GST-tag at N-terminal.
    Purification
    in vitro wheat germ expression system
    Top Product
    Discover our top product BSND Protéine
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Commentaires

    Preparation method: in vitro, wheat germ expression system
    Product Quality tested by: 12.5% SDS-PAGE Stained with Coomassie Blue.

    Restrictions
    For Research Use only
  • Buffer
    50 mM Tris-HCI, 10 mM reduced Glutathione, pH =8.0 in the elution buffer.
    Conseil sur la manipulation
    Aliquot to avoid repeated freezing and thawing.
    Stock
    -80 °C
    Stockage commentaire
    Best use within three months from the date of receipt of this protein.
  • Antigène
    BSND (Bartter Syndrome, Infantile, with Sensorineural Deafness (Barttin) (BSND))
    Autre désignation
    BSND (BSND Produits)
    Synonymes
    BSND Protein, BART Protein, DFNB73 Protein, Bartter syndrome, infantile, with sensorineural deafness (Barttin) Protein, barttin CLCNK type accessory beta subunit Protein, BSND Protein, Bsnd Protein
    Sujet
    Full Gene Name: Bartter syndrome, infantile, with sensorineural deafness (Barttin)
    Synonyms: BART,MGC119283,MGC119284,MGC119285
    ID gène
    7809
    NCBI Accession
    NM_057176
    Pathways
    Sensory Perception of Sound
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