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PEX26 Protein (AA 1-246) (His tag)

PEX26 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 90 % by SDS - PAGE SDS
N° du produit ABIN5853072
  • Antigène Voir toutes PEX26 Protéines
    PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 1-246
    Origine
    • 5
    • 2
    • 1
    Humain
    Source
    • 3
    • 2
    • 1
    • 1
    • 1
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette PEX26 protéine est marqué à la His tag.
    Application
    SDS-PAGE (SDS)
    Séquence
    MGSSHHHHHH SSGLVPRGSH MGSMKSDSST SAAPLRGLGG PLRSSEPVRA VPARAPAVDL LEEAADLLVV HLDFRAALET CERAWQSLAN HAVAEEPAGT SLEVKCSLCV VGIQALAEMD RWQEVLSWVL QYYQVPEKLP PKVLELCILL YSKMQEPGAV LDVVGAWLQD PANQNLPEYG ALAEFHVQRV LLPLGCLSEA EELVVGSAAF GEERRLDVLQ AIHTARQQQK QEHSGSEEAQ KPNLEGSVSH KFLSLPMLVR QLWDSAVSH
    Pureté
    > 90 % by SDS - PAGE
    Top Product
    Discover our top product PEX26 Protéine
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    Liquid. In 20  mM Tris-HCl buffer (  pH 8.0) containing 0.15M NaCl, 20 % glycerol, 1  mM DTT
    Stock
    4 °C,-20 °C,-80 °C
    Stockage commentaire
    Can be stored at +4C short term (1-2 weeks). For long term storage, aliquot and store at -20C or -70C. Avoid repeated freezing and thawing cycles.
  • Antigène
    PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))
    Autre désignation
    PEX26 (PEX26 Produits)
    Synonymes
    fk41g06 Protein, zgc:64014 Protein, wu:fk41g06 Protein, PBD7A Protein, PBD7B Protein, PEX26M1T Protein, Pex26pM1T Protein, 4632428M11Rik Protein, AI853212 Protein, peroxisomal biogenesis factor 26 Protein, peroxisomal biogenesis factor 26 L homeolog Protein, pex26 Protein, PEX26 Protein, pex26.L Protein, Pex26 Protein
    Sujet
    PEX26 belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene. Recombinant human PEX26 protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques.
    Poids moléculaire
    29.3 kDa (269aa), confirmed by MALDI-TOF
    NCBI Accession
    NP_001121121
    UniProt
    Q7Z412
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