Anti-CLEC5A Antibody (Rabbit Polyclonal antibody) General Information
Reacts with: Rat
Recombinant Rat CLEC5A / MDL1 / MDL-1 protein (Catalog#80259-R07H)
Produced in rabbits immunized with purified, recombinant Rat CLEC5A / MDL1 / MDL-1 (Catalog#80259-R07H; F7GAV1; Val30-Lys190). CLEC5A / MDL1 / MDL-1 specific IgG was purified by Rat CLEC5A / MDL1 / MDL-1 affinity chromatography.
Polyclonal Rabbit IgG
Protein A & Antigen Affinity
0.2 μm filtered solution in PBS
This antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.
Anti-CLEC5A Antibody (Rabbit Polyclonal antibody) Validated Applications
**********Please Note: Optimal concentrations/dilutions should be determined by the end user.**********
CLEC5A Background Information
CLEC5A, also known as MDL1 and MDL-1, is a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. CLEC5A with dnax-activation protein 12 and may play a role in cell activation. It also functions as a positive regulator of osteoclastogenesis. CLEC5A acts as a key regulator of synovial injury and bone erosion during autoimmune joint inflammation .The binding of dengue virus to CLEC5A triggers signaling through the phosphylation of TYROBP, this interaction does not result in viral entry, but stimulates proinflammatory cytokine release.
C-type lectin domain family 5, member A
Chen ST. et al., 2008, Nature. 453 (7195): 672-6. Davila S. et al., 2010, Genes Immun. 11 (3): 232-8. Hillier LW. et al., 2003, Nature. 424 (6945): 157-64.