| References |
| Synonyms |
|
| Formulation |
100 µg of protein G-purified IgG in 200 µg PBS containing 0.05% BSA and 0.05% sodium azide |
| Stability |
1 year |
| Storage |
-20°C |
| Shipping |
Wet ice
in continental US; may vary elsewhere
|
| Specificity |
| Human TLR8 |
+ |
| Murine TLR8 |
+ |
|
Background Reading
Chuang, T., and Ulevitch, R.J. Cloning and characterization of a sub-family of human toll-like receptors: hTLR7, hTLR8, and hTLR9. Eur Cytokine Netw 11(3) 372-378 (2000).
Du, X., Poltorak, A., Wei, Y., et al. Three novel mammalian toll-like receptors: Gene structure, expression, and evolution. Eur Cytokine Netw 11(3) 362-371 (2000).
Gibson, F.C., Hong, C., Chou, H., et al. Innate immune recognition of invasive bacteria accelerates atherosclerosis in apolipoprotein E-deficient mice. Circulation 109 2801-2806 (2004).
Srivastava, M.D., and Srivastava, B.I.S. Expression of mRNA and proteins for toll-like receptors, associated molecules, defensins and LL-37 by SRIK-NKL, a CD8+ NK/T cell line. Leuk Res 7 813-820 (2005).
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| Size |
Global Purchasing |
| 1 ea |
|
Description
Antigen:
synthetic peptide from human TLR8 within the region of amino acids 750-850
·
Host:
Mouse
·
Isotype:
IgG1κ
·
Application(s):
WB, FC (intracellular and cell surface), IHC (paraffin-embedded sections)
·
The toll-like receptors (TLRs) in mammals comprise a family of transmembrane proteins characterized by multiple copies of leucine rich repeats in the extracellular domain and an interleukin-1 (IL-1) receptor motif in the cytoplasmic domain. Like their counterparts in Drosophila, TLRs signal through adaptor molecules.1 The TLR family is a phylogenetically conserved mediator of innate immunity that is essential for microbial recognition.2 Most mammalian species have between ten and fifteen types of TLRs. Ten functional TLRs (TLR1-10) have been identified in human. Humans also encode a TLR11 gene but it contains several stop codons and protein is not expressed. However, mouse and rat TLR11 are functional, and it is thought that human TLR11 function was lost during evolution. Historically speaking, TLR expression has been most extensively studied in the immune system. Overall, TLRs are highly expressed in immune competent cells, including macrophages, dendritic cells, neutrophils, mucosal epithelial cells and dermal endothelial cells. However, TLRs have also been identified in many other cell types and anatomical tissue locations where they are expressed either constitutively or induced during infection. The TLR8 gene contains three exons, two of which have coding function.3 TLR8 cDNA codes for a protein of approximate molecular weight of 120 kDa.3,4
1
Srivastava, M.D., and Srivastava, B.I.S. Expression of mRNA and proteins for toll-like receptors, associated molecules, defensins and LL-37 by SRIK-NKL, a CD8+ NK/T cell line. Leuk Res 7 813-820 (2005).
2
Gibson, F.C., Hong, C., Chou, H., et al. Innate immune recognition of invasive bacteria accelerates atherosclerosis in apolipoprotein E-deficient mice. Circulation 109 2801-2806 (2004).
3
Du, X., Poltorak, A., Wei, Y., et al. Three novel mammalian toll-like receptors: Gene structure, expression, and evolution. Eur Cytokine Netw 11(3) 362-371 (2000).
4
Chuang, T., and Ulevitch, R.J. Cloning and characterization of a sub-family of human toll-like receptors: hTLR7, hTLR8, and hTLR9. Eur Cytokine Netw 11(3) 372-378 (2000).
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