Recombinant FANCM protein (His tag)

Recombinant FANCM protein (His tag)

Cat.#: 538456

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Product Information

  • Product Name
    Recombinant FANCM protein (His tag)
  • Documents
  • Description

    Recombinant Human Fanconi anemia group M protein (FANCM) fragment (residues 1818-2048) is a highly stable and soluble 231-amino acid segment ideal for structural and biochemical studies. This fragment, derived from the ATP-dependent RNA helicase FANCM, supports research into DNA repair mechanisms and Fanconi anemia pathways, offering a reliable tool for investigating protein interactions and enzymatic activities.

    The full-length FANCM protein is a DNA-dependent ATPase and key component of the Fanconi anemia (FA) core complex, essential for activating the FA pathway in response to DNA damage. It facilitates the monoubiquitination of the FANCI-FANCD2 complex, enhancing cellular resistance to DNA cross-linking agents and preventing chromosomal breakage. FANCM exhibits ATP-dependent DNA branch migration activity, processing branched DNA structures like replication forks, particularly when complexed with CENPS and CENPX. It also binds various DNA substrates, including single-strand DNA and splayed-arm DNA, in association with FAAP24. Localized to the nucleus, FANCM plays a critical role in genome maintenance and DNA repair, with implications for understanding Fanconi anemia and cancer biology.

  • Protein name
    Fanconi anemia group M protein
  • Uniprot ID
    Q8IYD8
  • Gene Name
    FANCM; KIAA1596
  • Source/Expression Host
    E. coli
  • Expression Plasmid/cDNA
    DNA encoding 1818-2048 aa (Q8IYD8) were fused with 6His tag.
  • Protein Species
    Human
  • Molecular weight
    Predictes a molecular mass of 28.07 kDa. In SDS-PAGE under reducing conditions, it migrates as an approximately 28 kDa band.
  • Purity
    >88%, by SDS-PAGE with Coomassie Brilliant Blue staining.
  • Activity
    Not tested.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"