highly pure (>98%) recombinant hIL-17F (human IL-17F)
形式Lyophilised:Reconstitute in sterile water to a concentration of 1.0 mg/ml Please note that if you receive this product in liquid form it has already been reconstituted as described and no further reconstitution is necessary.
存放说明Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term.
Constituents: PBS, pH 7.4
Concentration information loading...
纯度Immunogen affinity purified
纯化说明Anti-hIL-17F specific antibody was purified by affinity chromatography employing immobilized hIL-17F matrix.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Use a concentration of 0.5 µg/ml. In conjunction with compatible secondary reagents the detection limit of this antibody is 0.2 - 0.4 ng/well of recombinant hIL-17F.
Use a concentration of 0.1 - 0.2 µg/ml. Predicted molecular weight: 18 kDa.
功能Ligand for IL17RA and IL17RC (PubMed:17911633). The heterodimer formed by IL17A and IL17F is a ligand for the heterodimeric complex formed by IL17RA and IL17RC (PubMed:18684971). Involved in stimulating the production of other cytokines such as IL6, IL8 and CSF2, and in regulation of cartilage matrix turnover (PubMed:11591732, PubMed:11591768, PubMed:11574464). Also involved in stimulating the proliferation of peripheral blood mononuclear cells and T-cells and in inhibition of angiogenesis (PubMed:11591732). Plays a role in the induction of neutrophilia in the lungs and in the exacerbation of antigen-induced pulmonary allergic inflammation.
组织特异性Expressed in activated, but not resting, CD4+ T-cells and activated monocytes.
ab46000 (1µg/ml) staining IL17F in human ovary using an automated system (DAKO Autostainer Plus). Using this protocol there is strong staining of the cytoplasm of the corpus luteum. Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
Anti-IL17F antibody (ab46000)参考文献
has not yet been referenced specifically in any publications.