iF488 Anti-Mouse TCR β chain Antibody

Product Details


CloneH57-597-R1
ApplicationFlow Cytometry
ReactivityMouse
FormatiF488
Target NameTCR β chain, TCR-β
IsotypeRat IgG1
Antibody TypeMonoclonal
Regulatory StatusRUO
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and 0.2% (w/v) BSA
Protein ConcentrationSupplied at a lot-specific concentration.
Storage&HandlingThe antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
Recommended UsageFor flow cytometric staining, it is recommended to use 5 µL of this reagent per 0.5-1.0 million cells in a 100 µL volume. Optimal reagent performance should be determined by titration for each specific application. iF488 has an excitation max at 491 nm and an emission max at 516 nm.
Excitation LaserBlue Laser (488 nm)
RRIDAB_3739062
Research AreasAntigen presentation, T cells, T cell Activation
See All FormatsClone H57-597-R1

Background Information


The mouse T cell receptor (TCR) β chain is a critical component of the heterodimeric αβ TCR complex expressed on most mature T lymphocytes. Together with the TCR α chain, it confers antigen specificity to T cells, enabling the recognition of peptide fragments presented by major histocompatibility complex (MHC) molecules on antigen-presenting cells. This recognition event is essential for initiating adaptive immune responses, including T cell activation, proliferation, and differentiation into effector and memory subsets.

Structurally, the TCR β chain is composed of variable (V), diversity (D), joining (J), and constant (C) gene segments that undergo somatic recombination during T cell development in the thymus. This recombination process generates the highly variable complementarity-determining region 3 (CDR3), which contributes most significantly to antigen specificity. The β chain pairs non-covalently with the TCR α chain, forming the antigen-binding site. Each chain contains two extracellular immunoglobulin-like domains, a variable domain involved in antigen binding and a constant domain that stabilizes structure, along with a transmembrane segment and a short cytoplasmic tail. The TCR complex also associates with CD3 signaling molecules (CD3γ, CD3δ, CD3ε, and CD3ζ), which transduce activation signals through immunoreceptor tyrosine-based activation motifs (ITAMs).

The ligands for the mouse TCR β chain are peptide antigens bound to MHC class I or II molecules. Engagement of the αβ TCR with these peptide-MHC complexes triggers receptor conformational changes that initiate intracellular signaling cascades involving kinases such as Lck and ZAP-70, leading to T cell activation and effector function.

In disease, alterations in TCR β chain expression or repertoire diversity can contribute to immune dysfunction. Restricted TCR β repertoires are associated with autoimmune diseases, such as experimental autoimmune encephalomyelitis (EAE, a model for multiple sclerosis), and with impaired immune defense in infections or cancer. Somatic mutations or skewed TCR β usage have also been observed in T cell lymphomas and leukemia.

The mouse TCR β chain has significant therapeutic and experimental relevance. It serves as a model for studying clonal selection, antigen recognition, and tolerance mechanisms. In immunotherapy, manipulation of TCR β sequence diversity underpins TCR-engineered T cell strategies for cancer and infection control. Furthermore, analyzing mouse TCR β repertoires provides insights into vaccine efficacy, autoimmune mechanisms, and immune reconstitution following bone marrow transplantation.

Isotype Control


iF488 Rat IgG1 Isotype Control Antibody

Data Sheets


iF488 Anti-Mouse TCR β chain Antibody TDS

Related Protocols


Flow Cytometry Protocol

Related Products


APC Anti-Mouse TCR β chain Antibody, Clone H57-597-M2a

In Vivo Star Anti-Mouse TCR beta Antibody, Clone H57-597-m2a

Frequently Asked Questions


How do I determine the optimal antibody concentration/titer for my experiment?
We recommend titrating each new antibody lot on your own cell type and instrument, since optimal concentration depends on cell density, target expression level, and cytometer sensitivity. Suggested starting dilutions or test sizes (e.g., µg or µl per 10^6 cells) are provided on the product page as a starting reference point, not a fixed requirement.

Can these antibodies be used for intracellular or intranuclear staining, or only surface staining?
Intended use (surface, intracellular, or both) is specified per product, indicated under Application. The appropriate Related Protocol is linked for each product. If you need to detect both surface and intracellular markers in the same panel, confirm each antibody's compatibility with your fixation/permeabilization protocol before combining them.

What controls should I use alongside these antibodies?
Matched isotype controls (same host species, isotype, and conjugate) are available for most clones to help distinguish specific binding from background/non-specific staining and are linked on each product page. Unstained, single-color compensation, and fluorescence-minus-one (FMO) controls are also recommended, especially for multicolor panel design.

Can I combine InnoCyto Flow Cytometry antibodies into a multicolor panel?
Yes — antibodies across our catalog are designed to be panel-compatible, and conjugate options are offered specifically to support multiplexing. When building a panel, pair bright fluorophores with low-expression targets, avoid excessive spectral overlap, and confirm compensation is set up correctly for your specific fluorochrome combination. Use our Panel Builder to simplify the process.

Have a product or application question? Consult our FAQs or contact us.