Adipogen/anti-TLR5 (human), mAb (ABM22G1) (FITC)/AG-20T-0304F-C100/100 µg

作者: 时间:2025-01-31 点击量:

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Toll-like Receptor 5; Toll/interleukin-1 Receptor-like Protein 3; TIL3; MELIOS; SLE1; SLEB1
Monoclonal Antibody
ABM22G1
Mouse IgG2aκ
Recombinant human TLR5 protein (aa 261-420).
FITC
Flow Cytometry: (0.5μg/106 cells)Optimal conditions must be determined individually for each application.
Human
Recognizes human TLR5.
Protein G purified.
0.2mg/ml
Liquid. In 10mM TRIS containing 150mM NaCl and 0.05% sodium azide.
O60602
BLUE ICE
+4°C
+4°C
Do not freeze.Protect from light.
Stable for at least 6 months after receipt when stored at +4°C.
No
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TLR5 (Toll-like Receptor 5) is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLR5 recognizes bacterial flagellin, a principal component of bacterial flagella and a virulence factor, via a conserved region within flagellin, the D1 portion/domain. Binding of flagellin induces the dimerization of TLR5, which in turn recruits MyD88. The recruitment of MyD88 leads to subsequent activation of IRAK4, IRAK1, TRAF6 and eventually IκB kinases. Activation of IκB kinases mobilizes the nuclear factor NF-κB and stimulates many downstream gene expressions, which initiate the canonical proinflammatory pathway, including TNF-α production. TLR5 may play a role in inflammatory bowel disease (IBD). Lower levels of TLR5 expression have been found in patients exhibiting moderate to severe ulcerative colitis (UC). TLR5 is suggested to be possibly involved in HPV induced inflammation and subsequent cervical neoplasia formation. It has been reported that TLR5 expression is detected in both ovarian epithelium and ovarian cancer cell lines, suggesting a possible role of TLR5 in inflammation induced ovarian cancer onset. Mutations in this gene have been associated with both resistance and susceptibility to systemic lupus erythematosus and susceptibility to legionnaire disease, highlighting the importance of TLR5 in microbial recognition particularly at the mucosal surface.

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