Anti-Human CD31 (PECAM1) (Clone MGP7-11F10d) – Purified No Carrier Protein

Anti-Human CD31 (PECAM1) (Clone MGP7-11F10d) – Purified No Carrier Protein

Product No.: LTCC212

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Clone
MGP7-11F10d
Target
CD31 (PECAM-1)
Formats AvailableView All
Product Type
Hybridoma Monoclonal Antibody
Alternate Names
Platelet endothelial cell adhesion molecule; EndoCAM; GPIIA; PECA1; CD31
Isotype
Mouse IgG2a
Applications
immuno-MRM

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Antibody Details

Product Details

Reactive Species
Human
Host Species
HEK-293
Immunogen
N/A
Product Concentration
≥1.0 mg/ml
Purity
≥90% monomer by analytical SEC
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.
State of Matter
Liquid
Product Preparation
Purified antibodies are manufactured in an animal free facility using only in vitro protein free cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates.
Storage and Handling
This antibody may be stored sterile as received at 2-8°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.
Regulatory Status
Research Use Only
Country of Origin
USA
Shipping
2 – 8° C Wet Ice
Additional Applications Reported In Literature ?
immuno-MRM
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
MGP7-11F10d activity is directed against human PECAM1 (CD31), specifically the peptide sequence DQNFVILEFPVEEQDR.
Background
PECAM1 was the first immunoreceptor tyrosine-based inhibition motif (ITIM)-containing receptor to be identified in platelets and acts as a negative regulator of platelet activation1. Platelet activation from a resting state has broad implications for many pathophysiological processes, including anthogenesis, angiogenesis, inflammation, wound repair, and cancer metastasis. PECAM1 inhibits platelet activation and thrombosis at sites of vascular injury by attenuating immunoreceptor tyrosine-based activation motif (ITAM)-containing receptor complex GPVI-FcR γ-chain signaling and by acting as a positive regulator of αIIb β3-mediated outside-in signaling. PECAM1, like all ITIM-containing receptors, belongs to the immunoglobulin receptor superfamily.

PECAM1 also functions as a cell adhesion molecule and is capable of mediating calcium- dependent heterophilic aggregation2. Additionally, PECAM1 is expressed at cell-cell borders in the endocardial cells of the developing murine heart3. Because of its distribution pattern, PECAM1 is a target molecule for the delivery of antithrombotic agents4,5,6,7. Research is being conducted into the ability of PECAM1 to deliver drugs to the endothelium.

MGP7-11F10d was generated against human PECAM1 using mouse as the host species8. MGP7-11F10d targets the peptide sequence DQNFVILEFPVEEQDR and was developed for use in immuno-MRM assays.
Antigen Distribution
PECAM1 is expressed on the majority of nonerythroid hematopoietic cells, including platelets, monocytes, neutrophils, T cells, and B cell subsets as well as on vascular endothelium and the endocardial cells of developing heart tissue.
Ligand/Receptor
PECAM1 synthetic peptide BDKRB2
NCBI Gene Bank ID
UniProt.org
Research Area
Inflammatory Disease
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Cancer Research
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Immunoglobulins
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Platelet Activation

References & Citations

1 Coxon CH, Geer MJ, Senis YA. Blood. 129(26):3407-3418. 2017.
2 DeLisser HM, Yan HC, Newman PJ, et al. J Biol Chem. 268(21):16037-16046. 1993.
3 Baldwin HS, Shen HM, Yan HC, et al. Development. 120(9):2539-2553. 1994.
4 Muzykantov VR, Christofidou-Solomidou M, Balyasnikova I, et al. Proc Natl Acad Sci U S A. 96(5):2379-2384. 1999.
5 Scherpereel A, Wiewrodt R, Christofidou-Solomidou M, et al. FASEB J. 15(2):416-426. 2001.
6 Ding BS, Gottstein C, Grunow A, et al. Blood. 106(13):4191-4198. 2005.
7 Chacko AM, Nayak M, Greineder CF, et al. PLoS One. 7(4):e34958. 2012.
8https://research.fredhutch.org/content/dam/stripe/paulovich/files/PaulovichLab_Mab_AvailableForImmuno-MRM_11092020.pdf

Formats Available

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Disclaimer AlertProducts are for research use only. Not for use in diagnostic or therapeutic procedures.