Recombinant Mouse F11 Protein, His-tagged
Cat.No. : | F11-900M |
Product Overview : | Recombinant Mouse F11 Protein(Pro157~Arg389) was expressed in E.coli with N-terminal His Tag. |
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Source : | E. coli |
Species : | Mouse |
Tag : | His |
Form : | 20mM Tris, 150mM NaCl, pH8.0, containing 1mM EDTA, 1mM DTT, 0.01% SKL, 5% Trehalose and Proclin300. |
Molecular Mass : | 30kDa |
Protein length : | Pro157~Arg389 |
Purity : | >90% as determined by SDS-PAGE. |
Storage : | Avoid repeated freeze/thaw cycles. Store at 2-8°C for one month. Aliquot and store at -80°C for 12 months. |
Reconstitution : | Reconstitute in 20mM Tris, 150mM NaCl (pH8.0) to a concentration of 0.1-1.0 mg/mL. Do not vortex. |
Gene Name : | F11 coagulation factor XI [ Mus musculus ] |
Official Symbol : | F11 |
Synonyms : | F11; coagulation factor XI; PTA; plasma thromboplastin antecedent; FXI; Cf11; AI503996; 1600027G01Rik; |
Gene ID : | 109821 |
mRNA Refseq : | NM_028066 |
Protein Refseq : | NP_082342 |
Products Types
◆ Recombinant Protein | ||
F11-2914M | Recombinant Mouse F11 Protein, His (Fc)-Avi-tagged | +Inquiry |
F11-439M | Recombinant Mouse F11 Protein, MYC/DDK-tagged | +Inquiry |
F11-3602H | Recombinant Human F11 Protein, GST-tagged | +Inquiry |
F11-5333R | Recombinant Rat F11 protein, His&Myc-tagged | +Inquiry |
F11-2004H | Recombinant Human F11 Protein (19-387 aa), His-tagged | +Inquiry |
◆ Native Protein | ||
F11-2466H | Native Human Coagulation Factor XI | +Inquiry |
◆ Lysates | ||
F11-2681HCL | Recombinant Human F11 cell lysate | +Inquiry |
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Not For Human Consumption!
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Customer Reviews (3)
Write a reviewThe structure of the recombinant protein was analyzed by nuclear magnetic resonance (NMR), X-ray crystallography or electron microscopy, and the results showed that the protein was stable.
In the process of purification, the removal of impurities is good.
There are no structural or functional defects.
Q&As (6)
Ask a questionF11 plays an important role in diabetes, and abnormal levels may lead to insulin resistance and lipid metabolism disorders, which can lead to diabetes.
The mutation types of F11 include point mutations, insertions/deletions, duplications, etc., which may cause structural and functional abnormalities of the protein.
Studying the regulatory mechanism of F11 requires the comprehensive use of various experimental methods and techniques, such as gene knockout, transcriptome analysis, protein interaction, etc.
Abnormal F11 levels may indicate some diseases related to lipid metabolism, such as diabetes, obesity, hyperlipidemia, etc.
There are no drugs that directly regulate F11 levels, but they can be affected by lifestyle adjustments such as diet and exercise.
F11 has a complex relationship with other genes or proteins, and can interact with other genes or proteins and participate in a variety of biochemical reactions.
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