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Purified anti-LAT Antibody
Purified anti-LAT Antibody
623901 25 µg £54     
623902 100 µg £118     

Product Details

Clone: LAT1111
Isotype: Mouse IgG1
Reactivity: Human (does not cross-react with mouse)
Immunogen: Partial recombinant protein (cytoplasmic domain of human LAT)
Formulation: This LAT antibody is provided in phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide. Final antibody concentration is 0.5 mg/ml.
Preparation: The LAT antibody was purified by protein G affinity chromatography
Concentration: 0.5 mg/ml
Storage & Handling: Upon receipt, store frozen at 4° C.
Application:

WB-Quality tested
IP - Reported in the literature

Recommended Usage:

Each lot of this LAT antibody is quality control tested by Western blotting. Western blotting, suggested working dilution(s): Use 5 µg antibody per 5 ml antibody dilution buffer for each mini-gel. It is recommended that the reagent be titrated for optimal performance for each application.

COA:
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Whole cell extract from human
Whole cell extract from human peripheral blood mononuclear cells was resolved by electrophoresis, transferred to nitrocellulose and probed with monoclonal anti-LAT antibody. Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and a chemiluminescence system.


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Description:

LAT (linker for activation of T-cells) is a 36 kD phospho-tyrosine adaptor protein containing SH2 domains and a CVRC motif. Two LAT isoforms have been reported with approximate molecular weights of 36 kD and 38 kD. LAT is localized to lipid rafts, and is also a potential type III transmembrane protein, thought to be expressed in the juxtanuclear intracellular compartment. LAT links TCR engagement to Ras-MAPK activation, Ca2+ flux, IL-2 expression and is required for T-cell development. LAT is phosphorylated when activated by TCR cross-linking, where it recruits signaling molecules. LAT activation can be prevented by polyunsaturated fatty acids. LAT is modified by ZAP-70 and Syk phosphorylation and can also be palmitoylated. LAT has been reported to be associated with Grb2, Gads, Grap, PLC-γ1, p85 subunit PI3K, ZAP-70, Syk, Itk, Vav, SLP-76, and cbl. The LAT1111 monoclonal antibody recognizes the cytoplasmic domain of human LAT and has been shown to be useful for Western blotting and immunoprecipitation. The LAT1111 antibody does not cross-react with mouse LAT.

Other Names: Linker for activation of T-cells, 36 kD phospho-tyrosine adaptor protein
Structure: SH2 domains, CVRC motif; two isoforms 36 kD, 38 kD
Distribution: Lipid rafts, potential type III transmembrane protein, juxtanuclear intracellular compartment
Function: Links TCR engagement to Ras-MAPK activation, Ca2+ flux, IL-2 expression; required for T-cell development
Regulation: Phosphorylated when activated by TCR cross-linking, recruits signaling molecules, activation prevented by polyunsaturated fatty acids
Modification: Phosphorylation by ZAP-70, Syk, Palmitoylated
Interaction: Grb2, Gads, Grap, PLC-γ1, p85 subunit PI3K, ZAP-70, Syk, Itk, Vav, SLP-76, cbl
Antigen
References:

1. Zhang W, et al. 1998. Cell. 92:83.
2. Zeyda M, et al. 2002. J. Biol. Chem. 277:28418.
3. Perez-Villar J, et al. 2002 Biochemistry. 41:10732.
4. Hartgroves L, et al. 2003 J. Biol. Chem. 278:20389.

GeneID: 27040
Latest Publications: View the latest LAT articles on HighwirePress.com
UniProt: View information about LAT on UniProt.org
Keywords: Purified anti-LAT, LAT1111, Purified, Linker for activation of T-cells, 36 kD phospho-tyrosine adaptor protein, Human (does not cross-react with mouse), Immunology, Antibodies
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This data display is provided for general comparisons between formats. Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors. If you need assistance with selecting the best format contact our expert technical support team.

  • Purified anti-LAT
    Whole cell extract from human

    Whole cell extract from human peripheral blood mononuclear cells was resolved by electrophoresis, transferred to nitrocellulose and probed with monoclonal anti-LAT antibody. Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and a chemiluminescence system.

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