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Home > Antibodies > Anti-Mouse Antibodies (In Vivo) > Anti-Mouse PLVAP/PV-1 Monoclonal Antibodies

Anti-Mouse PLVAP/PV-1 Monoclonal Antibodies

PV1; Plasmalemma vesicle-associated protein; Plasmalemma vesicle protein 1

Catalog No. Product Name Size List Price (US$) Quantity
PA007476.r2a In vivo Grade Recombinant Anti-mouse PLVAP/PV-1 Monoclonal Antibody, Rat IgG2a Kappa (Clone: MECA-32) 1 mg 150.00
PA007476.r2a In vivo Grade Recombinant Anti-mouse PLVAP/PV-1 Monoclonal Antibody, Rat IgG2a Kappa (Clone: MECA-32) 5 mg 350.00
PA007476.r2a In vivo Grade Recombinant Anti-mouse PLVAP/PV-1 Monoclonal Antibody, Rat IgG2a Kappa (Clone: MECA-32) 25 mg 900.00
Description

PA007476.r2a: In vivo Grade Recombinant Anti-mouse PLVAP/PV-1 Monoclonal Antibody, Rat IgG2a Kappa (Clone: MECA-32)

Recombinant Rat IgG2a Kappa Monoclonal Antibody. 
Clone: MECA-32.
Isotype: Rat IgG2a Kappa.
Source: The anti-mouse PLVAP/PV-1 monoclonal antibody (clone: MECA-32) was produced in mammalian cells.
Specificity/Sensitivity: The in vivo grade recombinant rat monoclonal antibody (clone: MECA-32) specifically binds to the mouse PLVAP/PV-1 protein.
Applications: ELISA, flow cytometry, neutralization, functional assays such as bioanalytical PK and ADA assays, and those assays for studying biological pathways affected by the mouse PLVAP/PV-1 protein. 
Form of Antibody: 0.2 uM filtered solution, pH 7.4, no stabilizers or preservatives.
Endotoxin: < 1 EU per 1 mg of the protein by the LAL method.
Purity: >95% by SDS-PAGE under reducing conditions and HPLC.

Shipping: The In vivo Grade Recombinant Anti-mouse PLVAP/PV-1 Monoclonal Antibody, Rat IgG2a Kappa (Clone: MECA-32) is shipped with ice pack. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70°C as supplied.
1 month from date of receipt, 2 to 8°C as supplied.

 

References of anti-mouse PLVAP/PV-1 antibody (Clone: MECA-32):


Endothelial cell-derived angiopoietin-like protein 2 supports hematopoietic stem cell maintenance in the mouse bone marrow niche
Lin MI, et al. Stem Cells. 2022 Jan;40(1):80-91. doi: 10.1002/stem.3466. PMID: 34657340
Bone marrow sections were stained with MECA-32 antibody to identify endothelial cells in vivo. MECA-32+ ECs co-localized with Angptl2 in the BM niche. In vivo depletion of Angptl2 reduced HSC maintenance in the BM. MECA-32 staining confirmed vascular integrity in Angptl2-deficient mice. HSC frequency decreased in BM post-Angptl2 knockout.
Tags: anti-mouse PLVAP/PV-1 MECA-32; anti-mouse PLVAP/PV-1 MECA-32 antibody

VEGF-A modulates perivascular niche of human hematopoietic stem cells
Ding L, et al. Blood. 2018 Jun 7;131(23):2566-2576. doi: 10.1182/blood-2017-11-817171. PMID: 29754876
Vascular endothelial cells were labeled with MECA-32 antibody in vivo to assess VEGF-A effects. MECA-32+ vessels showed increased density post-VEGF-A administration. In vivo VEGF-A deletion disrupted perivascular HSC niches. HSC engraftment was impaired in VEGF-A-deficient BM. MECA-32 staining confirmed EC alterations in knockout mice.
Tags: anti-mouse PLVAP/PV-1 MECA-32 in vivo; anti-mouse PLVAP/PV-1 MECA-32 antibody in vivo

Endothelial cell-derived SLIT3 regulates intestinal stem cell regeneration
Aoki R, et al. J Clin Invest. 2017 Aug 1;127(8):3043-3056. doi: 10.1172/JCI93504. PMID: 28723562
Intestinal vasculature was stained with MECA-32 antibody to track ECs in vivo. MECA-32+ vessels supported ISC regeneration post-irradiation. In vivo SLIT3 deletion reduced vascular support for ISCs. MECA-32 staining revealed decreased vessel density in knockouts. ISC proliferation was impaired in SLIT3-deficient intestines.
Tags: anti-mouse PLVAP/PV-1 MECA-32 in animal model; anti-mouse PLVAP/PV-1 MECA-32 antibody in animal model

Endothelial-specific deletion of autophagy gene Atg7 suppresses tumorigenesis in a mouse model of liver cancer
Khambu B, et al. Hepatology. 2016 Jun;63(6):1837-49. doi: 10.1002/hep.28508. PMID: 26902621
Liver tumor vasculature was labeled with MECA-32 antibody for in vivo endothelial analysis. MECA-32+ ECs showed reduced density in Atg7-deficient tumors. In vivo Atg7 deletion suppressed tumor angiogenesis. Tumor growth was attenuated in endothelial-specific Atg7 knockouts. MECA-32 staining confirmed vascular defects in the tumor microenvironment.
Tags: anti-mouse PLVAP/PV-1 MECA-32 antibody in cancer research; anti-mouse PLVAP/PV-1 MECA-32 in mouse tumor model

Role of endothelial cells in early pancreas and liver development
Lammert E, et al. Mech Dev. 2013 Jan-Feb;130(1):44-50. doi: 10.1016/j.mod.2012.12.001. PMID: 23276718
Embryonic pancreatic tissues were stained with MECA-32 antibody to detect endothelial cells in vivo. MECA-32+ ECs were critical for early pancreatic bud formation. In vivo EC ablation disrupted liver and pancreas organogenesis. MECA-32 staining showed vascular networks in developing organs. Endothelial signals supported endocrine cell differentiation in vivo.
Tags: anti-mouse PLVAP/PV-1 antibody MECA-32; clone MECA-32 of anti-mouse PLVAP/PV-1 antibody

 

For more references about anti-mouse PLVAP/PV-1 antibody (Clone: MECA-32), please contact our scientific support team with message@sydlabs.com.

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