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ATP5F1D Protein (AA 43-161, partial) (GST tag)

ATP5F1D Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant 95 % ELISA
N° du produit ABIN7479168
  • Antigène Voir toutes ATP5F1D Protéines
    ATP5F1D (ATP synthase subunit delta, mitochondrial (ATP5F1D))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 43-161, partial
    Origine
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 4
    • 2
    • 2
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette ATP5F1D protéine est marqué à la GST tag.
    Application
    ELISA
    Séquence
    ASPTQVFFNG ANVRQVDVPT LTGAFGILAA HVPTLQVLRP GLVVVHAEDG TTSKYFVSSG SIAVNADSSV QLLAEEAVTL DMLDLGAAKA NLEKAQAELV GTADEATRAE IQIRIEANE
    Attributs du produit
    Please inquire if you are interested in this recombinant protein expressed in E. coli, mammalien cells or by baculovirus infection. Be aware about differences in price and lead time.
    Pureté
    95 %
    Top Product
    Discover our top product ATP5F1D Protéine
  • Commentaires

    The yeast protein expression system is the most economical and efficient eukaryotic system for secretion and intracellular expression. A protein expressed by the mammalian cell system is of very high-quality and close to the natural protein. But the low expression level, the high cost of medium and the culture conditions restrict the promotion of mammalian cell expression systems. The yeast protein expression system serve as a eukaryotic system integrate the advantages of the mammalian cell expression system. A protein expressed by yeast system could be modificated such as glycosylation, acylation, phosphorylation and so on to ensure the native protein conformation. It can be used to produce protein material with high added value that is very close to the natural protein. Our proteins produced by yeast expression system has been used as raw materials for downstream preparation of monoclonal antibodies.

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    0.2-2 mg/mL
    Buffer
    Tris-based buffer, 50 % glycerol
    Conseil sur la manipulation
    Repeated freezing and thawing is not recommended. Store working aliquots at 4 °C for up to one week
    Stock
    -20 °C
    Stockage commentaire
    Store at -20 °C for extended storage, conserve at -20 °C or -80 °C
  • Antigène
    ATP5F1D (ATP synthase subunit delta, mitochondrial (ATP5F1D))
    Autre désignation
    ATP synthase subunit delta, mitochondrial protein (ATP5F1D Produits)
    Synonymes
    fk58f09 Protein, zgc:73303 Protein, wu:fk58f09 Protein, MGC85306 Protein, GB17255 Protein, DDBDRAFT_0216607 Protein, DDBDRAFT_0238330 Protein, DDB_0216607 Protein, DDB_0238330 Protein, 0610008F14Rik Protein, 1500000I11Rik Protein, AA960090 Protein, AI876556 Protein, AU020773 Protein, C85518 Protein, ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit Protein, ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit L homeolog Protein, ATP synthase F1 delta Protein, atp5d Protein, atp5d.L Protein, ATP5D Protein, LOC552682 Protein, atp5D Protein, Atp5d Protein
    Sujet
    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 turnover in the catalytic domain of F1 is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Part of the complex F1 domain and of the central stalk which is part of the complex rotary element. Rotation of the central stalk against the surrounding alpha3beta3 subunits leads to hydrolysis of ATP in three separate catalytic sites on the beta subunits.
    Poids moléculaire
    39.8 kD
    UniProt
    P30049
    Pathways
    Proton Transport, Ribonucleoside Biosynthetic Process
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