Recombinant Rhesus monkey FEN1 Protein, His-tagged
Cat.No. : | FEN1-1687R |
Product Overview : | Recombinant Rhesus monkey FEN1 full length or partial length protein was expressed. |
- Specification
- Gene Information
- Related Products
Source : | Mammalian Cells |
Species : | Rhesus monkey |
Tag : | His |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method. |
Purity : | >80% |
Notes : | This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications. |
Storage : | Store it at +4 ºC for short term. For long term storage, store it at -20 ºC~-80 ºC. |
Storage Buffer : | PBS buffer |
Gene Name : | FEN1 flap structure-specific endonuclease 1 [ Macaca mulatta (Rhesus monkey) ] |
Official Symbol : | FEN1 |
Synonyms : | FEN1; flap endonuclease 1; |
Gene ID : | 722348 |
mRNA Refseq : | NM_001265950 |
Protein Refseq : | NP_001252879 |
MIM : | |
UniProt ID : | F7H3Z6 |
Products Types
◆ Recombinant Protein | ||
FEN1-1477H | Recombinant Human FEN1 Protein, His-tagged | +Inquiry |
Fen1-2986M | Recombinant Mouse Fen1 Protein, Myc/DDK-tagged | +Inquiry |
FEN1-1509R | Recombinant Rhesus Macaque FEN1 Protein, His (Fc)-Avi-tagged | +Inquiry |
FEN1-360H | Recombinant Human FEN1 protein(Met1~Thr195), His-tagged | +Inquiry |
FEN1-1971R | Recombinant Rat FEN1 Protein, His (Fc)-Avi-tagged | +Inquiry |
◆ Lysates | ||
FEN1-6264HCL | Recombinant Human FEN1 293 Cell Lysate | +Inquiry |
Related Gene
For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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Q&As (6)
Ask a questionMutations in the FEN1 protein can be detected and analyzed by methods such as whole-genome sequencing or target region sequencing to understand the impact of mutations on protein structure and function.
The FEN1 protein can be used as a biomarker in medical therapy to help monitor disease progression and treatment efficacy. In addition, therapeutics targeting the FEN1 protein, such as inhibiting its activity or regulating its expression, are also being investigated.
Abnormal levels of the FEN1 protein may suggest a genetic disorder such as cancer or neurofibroma, but it may also be associated with other diseases.
Studying the regulatory mechanism of FEN1 protein requires a combination of various experimental methods and techniques, such as gene knockout, transcriptome analysis, and protein-protein interactions.
Deficiency or aberrant expression of FEN1 protein may be associated with some cancers and genetic diseases, such as lung cancer, bowel cancer, neurofibromas, etc.
The types of mutations in the FEN1 protein include point mutations, insertions/deletions, duplications, etc., which may cause structural and functional abnormalities of the protein.
Customer Reviews (3)
Write a reviewFEN1 has strong stability.
It shows excellent stability in production.
FEN1 is easy to operate.
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