| Field | Specification |
|---|---|
| Mfr No | |
| Clonality | |
| Host | |
| Immunogen | E.coli-derived mouse Lat recombinant protein (Position: R29-E217) was used as the immunogen for the Lat antibody. |
| Isotype | |
| Product Type | |
| Purity | |
| Reactivity | |
| Storage | |
| Target | |
| UniProt # |
Overview
Lat Antibody / Linker for activation of T cells is a anti-Lat Rabbit antibody Polyclonal (rabbit origin) supplied in Lyophilized format. Recommended for workflows such as Western blot (WB), Immunohistochemistry (IHC), Flow cytometry (FACS), ELISA with listed reactivity in Mouse, Rat. Reported localization: Plasma membrane, Golgi.
Key elements and design rationale
- Target: Lat
- Antibody details: Rabbit, Polyclonal (rabbit origin), isotype Rabbit IgG
- Format: Lyophilized
- Applications (as listed): WB, IHC, FACS, ELISA
Biological background
Functionally, LAT antibody identifies a 233-amino-acid membrane protein that localizes to lipid rafts of the plasma membrane. Upon TCR stimulation, the Src-family kinase Lck and the ZAP-70 tyrosine kinase phosphorylate multiple tyrosine residues on LAT, creating docking sites for SH2-domain-containing proteins such as Grb2, PLC-gamma1, and Gads. These interactions recruit downstream effectors that activate calcium flux, MAPK signaling, and transcriptional pathways including NFAT, NF-kappaB, and AP-1. Through these mechanisms, LAT orchestrates the signal amplification necessary for full T-cell activation.
The LAT gene is located on chromosome 16p11.2 and encodes a single-pass type III transmembrane protein with a short extracellular domain and a cytoplasmic tail rich in tyrosine residues. The LAT scaffold acts as an organizational hub, integrating signals from the TCR, co-stimulatory receptors, and cytokine receptors. LAT phosphorylation dynamics are tightly regulated to prevent aberrant T-cell activation and autoimmunity. In developing thymocytes, LAT signaling contributes to both positive and negative selection, shaping the mature T-cell repertoire.
Defects in LAT expression or phosphorylation impair T-cell development and lead to severe combined immunodeficiency-like phenotypes. Conversely, gain-of-function mutations or dysregulated LAT signaling can cause hyperactivation syndromes, lymphoproliferative disorders, or autoimmunity. LAT also functions in mast cells, natural killer cells, and platelets, where it mediates Fc receptor-dependent signaling and degranulation responses.
LAT antibody is widely used in immunology, signal transduction, and cell biology research. It is suitable for western blotting, flow cytometry, and immunofluorescence to examine TCR-induced phosphorylation and signal complex formation. Researchers employ this antibody to dissect T-cell activation pathways and study immune regulation at the molecular level. LAT serves as a key marker of functional TCR signaling in both primary immune cells and model systems.
Structurally, LAT contains a cytoplasmic region with multiple phosphorylation sites that function as SH2-binding motifs for signaling partners. It forms large signalosomes through multivalent interactions that promote phase-separated clusters at the membrane.
Research relevance and current trends
- Connecting protein-level changes to phenotype using orthogonal readouts (genetic perturbation, transcriptomics, imaging).
- Considering isoforms and post-translational regulation when interpreting protein-level changes.
- Comparing results across species and model systems with matched controls.
Common research applications
- Western blotting: compare relative abundance and activation-state changes across conditions.
- Immunohistochemistry: map target signal in tissue context and compare regions/phenotypes.
- Flow cytometry: quantify target-positive populations and signal shifts at single-cell resolution.
- ELISA: support antibody-based quantification in assay formats where applicable.
Interpret changes in signal alongside appropriate controls and, when relevant, in parallel with total-protein or pathway readouts.
Notes for experimental interpretation
- Signal can reflect expression level, isoform composition, and post-translational state; interpret results in the context of your model system and stimuli.
- Species differences and sample matrices can influence epitope recognition; prioritize matched controls and orthogonal confirmation when feasible.
Antibody notes: Polyclonal antibodies recognize multiple epitopes, which can broaden the epitope footprint and may increase sensitivity in some contexts.
Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.