iF647 Anti-Human CD166 Antibody

Product Details


Clone3A6
ApplicationFlow Cytometry
ReactivityHuman
FormatiF647
Target NameCD166, CD6 ligand, Activated Leukocyte Cell Adhesion Molecule, ALCAM
IsotypeMouse 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. iF647 has an excitation max at 656 nm and an emission max at 670 nm.
Excitation LaserRed Laser (633 nm)
Research AreasAdhesion Molecules, Mesenchymal Stem cells, Activated T cells, B cells, Monocytes, Dendritic Cells, Vascular Endothelial cells, Cancer Marker, Angiogenesis
See All FormatsClone 3A6

Background Information


CD166, also known as activated leukocyte cell adhesion molecule (ALCAM), is a cell surface glycoprotein involved in cell–cell adhesion and immune regulation. It is broadly expressed on a variety of cell types, including activated T cells, monocytes, endothelial cells, epithelial cells, and certain stem and progenitor cells. CD166 plays an important role in mediating interactions between immune cells and between immune and non-immune cells, contributing to processes such as leukocyte trafficking, immune synapse formation, and tissue organization.

Structurally, CD166 is a type I transmembrane protein belonging to the immunoglobulin (Ig) superfamily. It contains five extracellular Ig-like domains (two variable-like and three constant-like domains), a single transmembrane region, and a short cytoplasmic tail. The extracellular domains mediate both homophilic interactions (CD166–CD166) and heterophilic binding, enabling flexible adhesion functions in different cellular contexts.

The principal ligand for CD166 is CD6, a receptor expressed on T cells. The CD166–CD6 interaction is critical for stabilizing the immunological synapse and enhancing T cell activation and proliferation. In addition to this heterophilic binding, CD166 can also engage in homophilic interactions, which contribute to cell aggregation and tissue integrity.

In disease, CD166 is implicated in cancer progression, inflammation, and autoimmune disorders. It is frequently overexpressed in a variety of malignancies, including colorectal, breast, prostate, and melanoma, where its expression is often associated with tumor invasion, metastasis, and poor prognosis. CD166 is also considered a marker of cancer stem cells in certain tumors. In inflammatory diseases, dysregulated CD166 expression may influence immune cell activation and tissue infiltration.

Therapeutically, CD166 is being investigated as a target for cancer treatment and immune modulation. Strategies include monoclonal antibodies, antibody-drug conjugates, and CAR T cell approaches aimed at eliminating CD166-expressing tumor cells. Additionally, modulating CD166–CD6 interactions may provide a means to regulate T cell responses in autoimmune diseases and transplantation. Ongoing research continues to explore its potential as both a biomarker and therapeutic target.

Isotype Control


iF647 Mouse IgG1 Isotype Control Antibody

Data Sheets


iF647 Anti-Human CD166 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.