ARG54702

anti-CD284 / TLR4 antibody

anti-CD284 / TLR4 antibody for Flow cytometry,Western blot and Human,Mouse,Rat

Cell Biology and Cellular Response antibody; Immune System antibody; Microbiology and Infectious Disease antibody
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Overview

Product Description Rabbit Polyclonal antibody recognizes CD284 / TLR4
Tested Reactivity Hu, Ms, Rat
Predict Reactivity Bov, Hm, Pig
Tested Application FACS, WB
Host Rabbit
Clonality Polyclonal
Target Name CD284 / TLR4
Antigen Species Human
Immunogen KLH-conjugated synthetic peptide corresponding to aa. 669-698 (Center) of Human TLR4 (NP_003257.1).
Conjugation Un-conjugated
Alternate Names CD284; CD antigen CD284; ARMD10; hToll; TLR-4; TOLL; Toll-like receptor 4

Application Instructions

Application Suggestion
Tested Application Dilution
FACS1:10 - 1:50
WB1:1000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Purification Protein A purified
Buffer PBS and 0.09% (W/V) Sodium azide
Preservative 0.09% (W/V) Sodium azide
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 21898 Mouse TLR4

GeneID: 29260 Rat TLR4

GeneID: 7099 Human TLR4

Gene Symbol TLR4
Gene Full Name toll-like receptor 4
Background The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This receptor has been implicated in signal transduction events induced by lipopolysaccharide (LPS) found in most gram-negative bacteria. Mutations in this gene have been associated with differences in LPS responsiveness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
Function Cooperates with LY96 and CD14 to mediate the innate immune response to bacterial lipopolysaccharide (LPS). Acts via MYD88, TIRAP and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response. Also involved in LPS- independent inflammatory responses triggered by free fatty acids, such as palmitate, and Ni(2+). Responses triggered by Ni(2+) require non-conserved histidines and are, therefore, species- specific. In complex with TLR6, promotes sterile inflammation in monocytes/macrophages in response to oxidized low-density lipoprotein (oxLDL) or amyloid-beta 42. In this context, the initial signal is provided by oxLDL- or amyloid-beta 42-binding to CD36. This event induces the formation of a heterodimer of TLR4 and TLR6, which is rapidly internalized and triggers inflammatory response, leading to the NF-kappa-B-dependent production of CXCL1, CXCL2 and CCL9 cytokines, via MYD88 signaling pathway, and CCL5 cytokine, via TICAM1 signaling pathway, as well as IL1B secretion. [From Uniprot]
Cellular Localization Cell membrane; Single-pass type I membrane protein. Note=Upon complex formation with CD36 and TLR6, internalized through dynamin-dependent endocytosis
Highlight Related products:
TLR4 antibodies; TLR4 ELISA Kits;
Related news:
Detecting exosomal HMGB1 for ICD research
Research Area Cell Biology and Cellular Response antibody; Immune System antibody; Microbiology and Infectious Disease antibody
Calculated MW 96 kDa
PTM N-glycosylated. Glycosylation of Asn-526 and Asn-575 seems to be necessary for the expression of TLR4 on the cell surface and the LPS-response. Likewise, mutants lacking two or more of the other N-glycosylation sites were deficient in interaction with LPS.

Images (2) Click the Picture to Zoom In

  • ARG54702 anti-CD284 / TLR4 antibody WB image

    Western blot: 30 µg of Jurkat, K562, PC3, HepG2, Raw264.7, NIH3T3, Mouse liver, Mouse ovary, Rat liver and Rat ovary lysates stained with ARG54702 anti-CD284 / TLR4 antibody at 1:500 dilution.

  • ARG54702 anti-CD284 / TLR4 antibody FACS image

    Flow Cytometry: U251 cells stained with ARG54702 anti-CD284 / TLR4 antibody (right histogram) or without primary antibody control (left histogram).

Customer's Feedback

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Review for anti-CD284 / TLR4 antibody

Application:WB

Sample:Transfected primary effusion lymphoma

Sample Loading Amount:45 μg

Primary Antibody Dilution Factor:1:1000

Primary Antibody Incubation Time:overnight

Primary Antibody Incubation Temperature:4 ºC

nuts_pic      Excellent

Review for anti-CD284 / TLR4 antibody

Application:WB

Sample:HeLa

Sample Loading Amount:30 µg

Primary Antibody Dilution Factor:1:500

Primary Antibody Incubation Time:overnight

Primary Antibody Incubation Temperature:4 ºC

Specific References

Mutation-Driven S100A8 Overexpression Confers Aberrant Phenotypes in Type 1 CALR-Mutated MPN

WB / Human

Ying-Hsuan Wang et al.
Int J Mol Sci.,  (2023)

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Electroacupuncture reduces blood glucose by regulating intestinal flora in type 2 diabetic mice

WB / Mouse

Jing An et al.
J Diabetes,  (2022)

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IL-37 inhibits the maturation of dendritic cells through the IL-1R8-TLR4-NF-κB pathway.

WB / Mouse

Liu Tianxiao et al.
Biochim Biophys Acta Mol Cell Biol Lipids.,  (2019)

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Anti-inflammatory effects of Ang-(1-7) via TLR4-mediated inhibition of the JNK/FoxO1 pathway in lipopolysaccharide-stimulated RAW264.7 cells.

WB / Mouse

Jiang Mei et al.
Dev Comp Immunol.,  (2018)

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Resistin facilitates breast cancer progression via TLR4-mediated induction of mesenchymal phenotypes and stemness properties.

WB / Human

Wang CH et al.
Oncogene.,  (2017)

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