FITC Anti-Human CD11c Antibody

Product Details


Clone011cAM1
ApplicationFlow Cytometry
ReactivityHuman
FormatFITC
Target NameCD11c, p150Integrin αx subunit, ITGAX, CR4
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. FITC has an excitation max at 493 nm and an emission max at 525 nm.
Excitation LaserBlue Laser (488 nm)
See All FormatsClone 011cAM1

Background Information


Human CD11c, also known as integrin alpha-X (ITGAX), is a cell-surface adhesion and immune-regulatory molecule predominantly expressed on dendritic cells, monocytes, macrophages, and subsets of B cells and other myeloid cells. CD11c forms a heterodimer with the integrin β2 subunit, CD18 (ITGB2), to create the complement receptor 4 (CR4) complex. Through interactions with extracellular matrix and immune-associated ligands, CD11c contributes to leukocyte adhesion, migration, phagocytosis, antigen presentation, and regulation of innate and adaptive immune responses.

CD11c is a large type I transmembrane glycoprotein containing an extracellular α-chain of approximately 1,163 amino acids, a single transmembrane region, and a relatively short cytoplasmic tail. Its major functional receptor is the CD11c/CD18 heterodimer. Known ligands include iC3b, fibrinogen, and several cell-surface and extracellular matrix molecules. Engagement of CD11c can regulate cytoskeletal organization, cell adhesion, phagocytosis, and intracellular signaling, although its effects depend strongly on the cellular context and activating signals.

CD11c is particularly important in immune-mediated diseases because it marks and participates in the function of activated myeloid and dendritic-cell populations. Altered CD11c-positive cell populations have been associated with autoimmune diseases such as rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, and multiple sclerosis. CD11c-positive tumor-associated myeloid cells can also influence tumor immunity, potentially contributing either to anti-tumor responses or immunosuppressive tumor microenvironments.

Therapeutically, CD11c represents an attractive target for selectively modulating dendritic cells and other myeloid populations. Antibody-drug conjugates, antibody-mediated depletion strategies, and CD11c-targeted antigen-delivery systems have been investigated for cancer, autoimmunity, and vaccine development. Rather than simply blocking CD11c signaling, targeted delivery through CD11c may provide a way to selectively manipulate antigen-presenting cells and enhance immune responses.

Isotype Control


FITC Mouse IgG1 Isotype Control Antibody

Data Sheets


FITC Anti-Human CD11c 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.