Anti-FA9/ F9/ F9 p22 monoclonal antibody
Anti-FA9/ F9/ F9 p22 antibody for FACS & in-vivo assay
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(antibodies, antigen, VLP, mRNA, ORF viral vector, etc)
Product information
Catalog No. | Product Name | Species Reactivity |
---|---|---|
GM-Tg-hg-T83369-Ab-1/ GM-Tg-hg-T83369-Ab-2 | Anti-Human F9 monoclonal antibody | Human |
GM-Tg-rg-T83369-Ab-1/ GM-Tg-rg-T83369-Ab-2 | Anti-Rat F9 monoclonal antibody | Rat |
GM-Tg-mg-T83369-Ab-1/ GM-Tg-mg-T83369-Ab-2 | Anti-Mouse F9 monoclonal antibody | Mouse |
GM-Tg-cynog-T83369-Ab-1/ GM-Tg-cynog-T83369-Ab-2 | Anti-Cynomolgus/ Rhesus macaque F9 monoclonal antibody | Cynomolgus/ Rhesus macaque |
GM-Tg-felg-T83369-Ab-1/ GM-Tg-felg-T83369-Ab-2 | Anti-Feline F9 monoclonal antibody | Feline |
GM-Tg-cang-T83369-Ab-1/ GM-Tg-cang-T83369-Ab-2 | Anti-Canine F9 monoclonal antibody | Canine |
GM-Tg-bovg-T83369-Ab-1/ GM-Tg-bovg-T83369-Ab-2 | Anti-Bovine F9 monoclonal antibody | Bovine |
GM-Tg-equg-T83369-Ab-1/ GM-Tg-equg-T83369-Ab-2 | Anti-Equine F9 monoclonal antibody | Equine |
Size: 1mg | 10mg | 100mg
Product Description
Catalog No. | GM-Tg-hg-T83369-Ab-1/ GM-Tg-hg-T83369-Ab-2; GM-Tg-rg-T83369-Ab-1/ GM-Tg-rg-T83369-Ab-2; GM-Tg-mg-T83369-Ab-1/ GM-Tg-mg-T83369-Ab-2; GM-Tg-cynog-T83369-Ab-1/ GM-Tg-cynog-T83369-Ab-2; GM-Tg-felg-T83369-Ab-1/ GM-Tg-felg-T83369-Ab-2; GM-Tg-cang-T83369-Ab-1/ GM-Tg-cang-T83369-Ab-2; GM-Tg-bovg-T83369-Ab-1/ GM-Tg-bovg-T83369-Ab-2; GM-Tg-equg-T83369-Ab-1/ GM-Tg-equg-T83369-Ab-2 |
Products Name | Anti-F9 monoclonal antibody |
Format | mab |
Target Name | F9 |
Protein Sub-location | Transmembrane Protein |
Category of antibody | FACS/Biofunctional Antibody, Therapeutics Target antibody |
Derivation (species) | Mouse |
CH1+2+3 Isotype (Receptor identification) | IgG |
Type of Light Chain (VD-LC) | N/A |
Expression platform | Mammalian Expression |
Bioactivity validation | Binding affinity is validated by using flow cytometry with antigen overexpressed cell line. The biofunction of antibodies are validated in cell-based assay (IC50 or EC50 TBD). |
Tag | Fc |
Products description | Pre-made anti-F9 benchmark inhibitory monoclonal antibody(mab) (blocking antibody inhibitor) is expressed by mammalian cell line as a benchmark antibody for cell culture, FACS,ELISA or other affinity binding assay or functional assay development, animal model development, PK/PD model development (Pharmacokinetics & Pharmacodynamic) |
Purity | Purity: ≥95% (SDS-PAGE) |
Application | Biological drug disovery including cell culture, assay development, animal model development, PK/PD model development (Pharmacokinetics & Pharmacodynamic) and mechanism of action (MOA) research. |
Formulation & Reconstitution | Lyophilized from GM's Protein Stability Buffer2 (PSB2,Confidential Ingredients) or PBS (pH7.4); For PSB2, reconstituted with 0.9% sodium chloride; For PBS, reconstituted with ddH2O. |
Storage | Store at -20℃ to -80℃ under sterile conditions. Avoid repeated freeze-thaw cycles. |
Reference
Data / case study
Click to get more Data / Case study about the product.
Associated products
Target information
Target ID | GM-T83369 |
Target Name | F9 |
Gene ID | 2158,14071,24946,695578,404015,493973,100054449 |
Gene Symbol and Synonyms | Cf-9,Cf9,F9,F9 p22,FIX,HEMB,P19,PTC,THPH8 |
Uniprot Accession | P00740,P16296,P19540,Q6SA95 |
Uniprot Entry Name | FA9_HUMAN,FA9_RAT,FA9_FELCA,FA9_CANLF |
Protein Sub-location | Transmembrane Protein |
Category | Therapeutics Target, INN Index |
Disease | N/A |
Gene Ensembl | ENSG00000101981 |
Target Classification | N/A |
The target: F9, gene name: F9, also named as F9 p22, FIX, HEMB, P19, PTC, THPH8. This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Sep 2015].
About Gmab
GMab, developed by GeneMedi, constitutes an advanced library of recombinant monoclonal antibodies, each meticulously designed to target specific molecular entities. Leveraging the sophisticated capabilities of GM’s Taurus™ and LIBRA™ platforms, GMab synthesizes antibodies characterized by high binding affinity, exceptional physicochemical stability, and optimal developability profiles.
Through expression in mammalian cell lines, GMab has been established as a paradigmatic reference antibody. It holds significance in myriad domains of biological drug discovery, encompassing cellular cultivation, innovative assay methodologies, strategic animal model systematization, in-depth pharmacokinetic & pharmacodynamic (PK/PD) modeling, and intricate mechanism of action (MOA) investigations.