Recombinant Human FANCM Protein: FAQs & Key Facts
Recombinant Human FANCM Protein: FAQs & Key Facts
Recombinant Human FANCM Protein is a recombinant form of the Fanconi anemia complementation group M protein, a key DNA helicase/translocase involved in the Fanconi anemia DNA damage response pathway, offered by Aladdin Scientific (SKU: rp366912) to support research into DNA repair mechanisms and genomic stability.
- Product Name
- Recombinant Human FANCM Protein
- SKU
- rp366912
- Gene / Protein
- FANCM (Fanconi Anemia Complementation Group M)
- Protein Function
- ATP-dependent DNA helicase/translocase; central scaffold of the Fanconi anemia core complex involved in interstrand crosslink repair
- Species
- Human (Homo sapiens)
- Recommended Storage
- Store at -80 °C; avoid repeated freeze-thaw cycles (flag: verify with datasheet)
- Supplier
- Aladdin Scientific
What Is Recombinant Human FANCM Protein?
Recombinant Human FANCM Protein (SKU: rp366912) is a recombinant form of the human FANCM gene product, a member of the Fanconi anemia (FA) complementation group. FANCM encodes an ATP-dependent DNA helicase and branch-point translocase that acts as a central component of the FA core complex. This complex is essential for the monoubiquitination of FANCD2 and FANCI, which in turn activates downstream DNA repair processes to resolve DNA interstrand crosslinks (ICLs).
FANCM is unique among FA proteins because it directly engages DNA substrates via its DEAH-box helicase domain and can remodel stalled replication forks. Its scaffold function recruits additional FA and non-FA repair factors to sites of DNA damage, making it indispensable for maintaining genomic integrity.
What Are the Key Research Applications?
Recombinant Human FANCM Protein is suitable for a range of biochemical and cell biology research applications, including:
- In vitro helicase and ATPase activity assays: Characterizing the enzymatic properties of FANCM or testing the effect of small-molecule inhibitors on its activity.
- Protein–protein interaction studies: Investigating FANCM interactions with FA core complex partners (e.g., FAAP24, MHF1/MHF2) using pull-down or co-immunoprecipitation assays.
- DNA-binding and branch migration assays: Using synthetic Holliday junction or replication fork substrates to study FANCM translocase activity.
- Western blotting and ELISA standards: As a positive control or standard for immunodetection assays.
Note: Verify specific validated applications on the product datasheet prior to use.
Storage, Handling, and Quality Considerations
Proper storage and handling are critical to preserving the activity and integrity of Recombinant Human FANCM Protein:
- Temperature: Store at -80 °C upon receipt. Short-term storage at -20 °C may be acceptable depending on formulation; consult the product datasheet for confirmed conditions.
- Freeze-thaw cycles: Minimize freeze-thaw cycles by preparing single-use aliquots. Repeated freezing and thawing can denature the protein and reduce enzymatic activity.
- Carrier protein: If the formulation includes BSA or glycerol as a stabilizer, ensure compatibility with your downstream assay before use.
- Purity and quality control: Recombinant proteins from Aladdin Scientific undergo SDS-PAGE and/or other QC analyses to confirm expected molecular weight and purity. Refer to the Certificate of Analysis (CoA) for lot-specific data.
Flag: Specific storage buffer composition, purity percentage, and molecular weight should be verified against the official product datasheet and CoA for SKU rp366912.
Ordering and Technical Support
Recombinant Human FANCM Protein (SKU: rp366912) is available for order directly from Aladdin Scientific. To place an order or request a quote:
- Visit the Aladdin Scientific website and search by SKU rp366912.
- Contact your regional Aladdin Scientific sales representative for bulk pricing, custom formulations, or special requirements.
- For technical questions regarding experimental design, protein activity, or compatibility, reach out to Aladdin Scientific's technical support team.
Certificates of Analysis (CoA) and Safety Data Sheets (SDS) are available on the product page or upon request from customer service. For returns or product quality concerns, please refer to Aladdin Scientific's return and refund policy.
Frequently asked questions
What is the biological function of FANCM protein?
FANCM is an ATP-dependent DNA helicase and branch-point translocase that serves as a central scaffold of the Fanconi anemia (FA) core complex. It plays a critical role in remodeling stalled replication forks and facilitating the monoubiquitination of FANCD2/FANCI, which activates the FA DNA damage response pathway to repair interstrand crosslinks (ICLs) and maintain genomic stability.
What applications is Recombinant Human FANCM Protein (rp366912) validated for?
Recombinant Human FANCM Protein is generally suited for in vitro enzymatic activity assays (helicase and ATPase assays), protein–protein interaction studies, DNA-binding and branch migration assays, and as a positive control in Western blot or ELISA experiments. Please consult the official product datasheet for the complete and confirmed list of validated applications for SKU rp366912.
How should Recombinant Human FANCM Protein be stored to maintain activity?
The protein should be stored at -80 °C immediately upon receipt to maintain stability and enzymatic activity. To prevent degradation, prepare single-use aliquots to minimize freeze-thaw cycles. Always refer to the product datasheet and Certificate of Analysis for lot-specific storage recommendations and formulation details.
Is Recombinant Human FANCM Protein suitable for use as a Western blot positive control?
Recombinant Human FANCM Protein can be used as a positive control in Western blotting assays to verify antibody specificity and assay performance. Confirm the expected molecular weight and recommended loading amount from the product datasheet prior to use.
What is the significance of FANCM in cancer and disease research?
Mutations or dysregulation of FANCM are associated with Fanconi anemia, a rare inherited disorder characterized by bone marrow failure and elevated cancer susceptibility. FANCM is also implicated in broader cancer biology, as its role in replication fork stabilization and ICL repair makes it a potential target for studying chemotherapy resistance mechanisms and synthetic lethality strategies.
References
- Meetei AR, et al. A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nature Genetics, 2005.
- Huang J, et al. The FANCM/FAAP24 complex is required for the DNA interstrand crosslink-induced checkpoint response. Molecular Cell, 2010.
- Aladdin Scientific. Recombinant Human FANCM Protein, SKU rp366912. Product Datasheet.
Products are supplied for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
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