Anti-Mouse CD279 (PD-1) (Clone RMP1-14) - Purified in vivo PLATINUM™ Functional Grade

Cat# P372-25

Size : 25mg

Brand : Leinco Technologies

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AntiMouse CD279 (PD1) (Clone RMP114) – Purified in vivo PLATINUM™ Functional Grade

Product No.: P372

[product_table name="All Top" skus="P372"]

Clone
RMP114
Target
PD1
Formats AvailableView All
Product Type
Monoclonal Antibody
Alternate Names
Programmed Death1, CD279, PD 1
Isotype
Rat IgG2a κ
Applications
B
,
FA
,
FC
,
IHC
,
in vivo
,
WB

Data

Antibody Details

Product Details

Reactive Species
Mouse
Host Species
Rat
Recommended Isotype Controls
Recommended Isotype Controls
Recommended Dilution Buffer
Immunogen
Mouse PD1 transfected BHK cells
Product Concentration
≥7.0 mg/ml
Endotoxin Level
<0.5 EU/mg as determined by the LAL method
Purity
≥95% monomer by analytical SEC
>95% by SDS Page
Formulation
This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration.
Product Preparation
Functional grade preclinical antibodies are manufactured in an animal free facility using in vitro cell culture techniques and are purified by a multistep process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates.
Pathogen Testing
To protect mouse colonies from infection by pathogens and to assure that experimental preclinical data is not affected by such pathogens, all of Leinco’s Purified Functional PLATINUM™ antibodies are tested and guaranteed to be negative for all pathogens in the IDEXX IMPACT I Mouse Profile.
Storage and Handling
Functional grade preclinical antibodies may be stored sterile as received at 28°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ 70°C. Avoid Repeated Freeze Thaw Cycles.
Country of Origin
USA
Shipping
Next Day 28°C
Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change.

Description

Description

Specificity
Clone RMP114 recognizes an epitope on mouse PD1.
Background
PD1 is a 5055 kD member of the B7 Ig superfamily. PD1 is also a member of the extended CD28/CTLA4 family of T cell regulators and is suspected to play a role in lymphocyte clonal selection and peripheral tolerance. The ligands of PD1 are PDL1 and PDL2, and are also members of the B7 Ig superfamily. PD1 and its ligands negatively regulate immune responses. PDL1, or B7Homolog 1, is a 40 kD type I transmembrane protein that has been reported to costimulate T cell growth and cytokine production. The interaction of PD1 with its ligand PDL1 is critical in the inhibition of T cell responses that include T cell proliferation and cytokine production. PDL1 has increased expression in several cancers. Inhibition of the interaction between PD1 and PDL1 can serve as an immune checkpoint blockade by improving Tcell responses In vitro and mediating preclinical antitumor activity. Within the field of checkpoint inhibition, combination therapy using antiPD1 in conjunction with antiCTLA4 has significant therapeutic potential for tumor treatments. PDL2 is a 25 kD type I transmembrane ligand of PD1. Via PD1, PDL2 can serve as a coinhibitor of T cell functions. Regulation of T cell responses, including enhanced T cell proliferation and cytokine production, can result from mAbs that block the PDL2 and PD1 interaction.
Antigen Distribution
PD1 is expressed on a subset of CD4CD8 thymocytes, and on activated T and B cells.
Ligand/Receptor
PDL1 (B7H1), PDL2
Function
Lymphocyte clonal selection, peripheral tolerance
NCBI Gene Bank ID
Research Area
Apoptosis
.
Cancer
.
Cell Biology
.
Cell Death
.
Immunology
.
Inhibitory Molecules
.
Tumor Suppressors

References & Citations

1.) Ardolino, M. et al. (2018) J Clin Invest. 128(10):46544668. PubMed
2.) Schreiber, RD. et al. (2017) Cancer Immunol Res. 5(2):106117.
3.) Honjo, T. et al. (1992) EMBO J. 11:3887.
4.) Gubin et al. (2018) Cell. 175:1014–1030 Journal Link
5.) Renner et al. (2019) Cell Reports. 29:135–150 Journal Link
6.) Gubin, M. et al. (2018) Cell 175(4):10141030.e19 Journal Link

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