APC Anti-mouse CD279 (PD-1) Antibody

Product Details


Clone29F.1A12
ApplicationFlow Cytometry, IHC-F
ReactivityMouse
FormatAPC
Target NameCD279, Programmed Death-1, PD 1, PDCD1, PD-1
IsotypeRat IgG2a
Antibody TypeMonoclonal
Regulatory StatusRUO
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and 0.2% (w/v) BSA
Protein Concentration0.2 mg/mL
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 less than 0.25 µg 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. PE/Cyanine7 has an excitation max at 565 nm and an emission max at 774 nm.
Excitation LaserRed Laser (633 nm)
See All FormatsClone 29F.1A12

Background Information


Mouse CD279, more commonly known as programmed cell death protein 1 (PD-1), is an inhibitory immune checkpoint receptor expressed primarily on activated T cells, as well as B cells and some myeloid populations. It plays a critical role in maintaining peripheral tolerance and preventing excessive immune activation by downregulating T cell responses during chronic antigen exposure, such as infection or inflammation. PD-1 is rapidly induced following T cell receptor engagement and acts as a key regulator of immune homeostasis.


Structurally, PD-1 is a type I transmembrane protein belonging to the immunoglobulin superfamily. It contains a single extracellular IgV-like domain responsible for ligand binding, a transmembrane region, and a cytoplasmic tail with immunoreceptor tyrosine-based inhibitory (ITIM) and switch (ITSM) motifs. Upon ligand engagement, these motifs recruit phosphatases such as SHP-2, which attenuate proximal T cell receptor signaling pathways.


The primary ligands of PD-1 are PD-L1 (CD274) and PD-L2 (CD273), which are expressed on antigen-presenting cells and various non-hematopoietic tissues. Interaction of PD-1 with its ligands suppresses T cell proliferation, cytokine production, and survival, promoting an exhausted T cell phenotype during chronic immune stimulation.


PD-1 signaling is implicated in chronic infections, cancer, and autoimmune diseases. In tumors, PD-1-mediated inhibition allows cancer cells to evade immune surveillance by suppressing anti-tumor T cell activity.


Therapeutically, blockade of the PD-1/PD-L1 axis using monoclonal antibodies has revolutionized cancer immunotherapy by restoring T cell function. Conversely, enhancing PD-1 signaling may be beneficial in treating autoimmune diseases and preventing transplant rejection, making it a versatile target in immune modulation.

Isotype Control


APC Rat IgG2a Isotype Control

Data Sheets


APC Anti-mouse CD279 (PD-1) 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.