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CF59

Recombinant Human E3 ubiquitin-protein ligase parkin/PARK2/PRKN

10ug

1200

1080

现货

国产

CF59

Recombinant Human E3 ubiquitin-protein ligase parkin/PARK2/PRKN

50ug

3520

3168

现货

国产

CF59

Recombinant Human E3 ubiquitin-protein ligase parkin/PARK2/PRKN

500ug

13440

12096

现货

国产

CF59

Recombinant Human E3 ubiquitin-protein ligase parkin/PARK2/PRKN

1mg

19200

17280

现货

国产

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  • Catalog# CF59
    Source E.coli
    Description Recombinant Human Parkinson Juvenile Disease Protein 2/PARK2 is produced with our E. coli expression system. The target protein is expressed with sequence (Met1-Lys387) of Human PARK2 fused with a 6His tag at the C-terminus.
    Names E3 Ubiquitin-Protein Ligase Parkin, Parkinson Juvenile Disease Protein 2, Parkinson Disease Protein 2, PARK2, PRKN
    Accession # O60260-5
    Formulation Supplied as a 0.2 μm filtered solution of PBS, 20% Glycerol, 2mM DTT, pH 7.4
    Shipping The product is shipped on dry ice/ice packs.
    Storage Store at < -20°C, stable for 6 months after receipt.
    Please minimize freeze-thaw cycles.
    Biological Activity IN STOCK
    Purity Greater than 95% as determined by SEC-HPLC and reducing SDS-PAGE.
    Endotoxin Less than 0.1 ng/µg (1 IEU/µg).
    Amino Acid Sequence
    MIVFVRFNSSHGFPVEVDSDTSIFQLKEVVAKRQGVPADQLRVIFAGKELRNDWTVQNCDLDQQS IVHIVQRPWRKGQEMNATGGDDPRNAAGGCEREPQSLTRVDLSSSVLPGDSVGLAVILHTDSRKD SPPAGSPAGRSIYNSFYVYCKGPCQRVQPGKLRVQCSTCRQATLTLTQGPSCWDDVLIPNRMSGE CQSPHCPGTSAEFFFKCGAHPTSDKETSVALHLIATNSRNITCITCTDVRSPVLVFQCNSRHVIC LDCFHLYCVTRLNDRQFVHDPQLGYSLPCVGTGDTVVLRGALGGFRRGVAGCPNSLIKELHHFRI LGEEQYNRYQQYGAEECVLQMGGVLCPRPGCGAGLLPEPDQRKVTCEGGNGLGCGYGQRRTKLEH HHHHH
    Background E3 Ubiquitin-Protein Ligase Parkin (PARK2) belongs to the RBR family and Parkin subfamily. PARK2 is expressed in the heart, testis, skeletal muscle, with high expression levels found in the brain including the substantianigra. PARK2 is a component of a multiprotein E3 ubiquitin ligase complex that mediates the targeting of substrate proteins for proteasomal degradation. The mutations of gene encoding this protein will result in Parkinson disease and autosomal recessive juvenile Parkinson disease.