iF647 Anti-Mouse CD90.2 (Thy1.2) Antibody

Product Details


Clone30-H12
ApplicationFlow Cytometry
ReactivityMouse
FormatiF647
Target NameCD90.2, Thy1.2, Thy-1.2
IsotypeRat IgG2b
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. iF647 has an excitation max at 656 nm and an emission max at 670 nm.
Excitation LaserRed Laser (633 nm)
Research AreasT cells, Hematopoietic Stem Cells, Neurons
See All FormatsClone 30-H12

Background Information


Mouse CD90.2, also known as Thy-1.2, is a glycosylphosphatidylinositol (GPI)-anchored cell surface glycoprotein that belongs to the immunoglobulin superfamily. It is widely expressed in mice on several cell types, including thymocytes, mature T lymphocytes, neurons, fibroblasts, and some stem or progenitor cells. In immunology research, CD90.2 serves as an important marker for identifying mouse T cells and distinguishing mouse strains that express the Thy-1.2 allele from those expressing the alternative Thy-1.1 allele.

Structurally, CD90.2 is a relatively small protein of approximately 25–37 kDa depending on glycosylation. It contains a single extracellular immunoglobulin-like domain, multiple glycosylation sites, and is attached to the outer leaflet of the plasma membrane through a GPI anchor rather than a transmembrane region. Because it lacks an intracellular domain, CD90.2 does not signal directly but instead participates in signaling through associations with other membrane proteins and lipid raft microdomains. This arrangement allows CD90.2 to influence cell–cell interactions and intracellular signaling pathways indirectly.

Although the precise physiological ligands of CD90 are not completely defined, studies have shown that Thy-1 molecules can interact with integrins, such as αvβ3 integrin, on neighboring cells. These interactions contribute to cell adhesion, communication between immune cells and stromal cells, and regulation of cell activation and migration.

CD90 plays roles in immune regulation, neuronal development, and tissue repair. Abnormal CD90 expression has been associated with inflammatory conditions, fibrosis, and certain cancers, where it may influence cell proliferation and tumor–stromal interactions. In therapeutic research, CD90 is used as a marker to isolate specific cell populations, including T cells and stem cells. Antibodies against CD90.2 are widely used in mouse models for immune cell depletion, cell tracking, and transplantation studies.

Isotype Control


iF647 Rat IgG2b Isotype Control

Data Sheets


iF647 Anti-Mouse CD90.2 (Thy1.2) Antibody TDS

Related Protocols


Flow Cytometry Protocol

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.