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HPA039980

Sigma-Aldrich

Anti-NRP2 antibody produced in rabbit

Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution

Synonyme(s) :

Anti-Neuropilin 2, Anti-Vegf165r2

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About This Item

Numéro MDL:
Code UNSPSC :
12352203
Numéro HPA (Human Protein Atlas):
Nomenclature NACRES :
NA.43

Source biologique

rabbit

Conjugué

unconjugated

Forme d'anticorps

affinity isolated antibody

Type de produit anticorps

primary antibodies

Clone

polyclonal

Gamme de produits

Prestige Antibodies® Powered by Atlas Antibodies

Forme

buffered aqueous glycerol solution

Espèces réactives

human

Technique(s)

immunohistochemistry: 1:500-1:1000

Séquence immunogène

LSLTFHTDMAVAKDGFSARYYLVHQEPLENFQCNVPLGMESGRIANEQISASSTYSDGRWTPQQSRLHGDDNGWTPNLDSNKEYL

Numéro d'accès UniProt

Conditions d'expédition

wet ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... NRP2(8828)

Description générale

The gene NRP2 (neuropilin 2) is mapped to human chromosome 2q33. The gene encodes a single-spanning transmembrane glycoprotein. It belongs to the NRP class of proteins. The protein has two CUB (complement C1r/C1s, Uegf, Bmp1) domains, two F5/8 domains, a MAM (meprin/A5 protein/receptor protein tyrosine phosphatase μ) domain and a transmembrane region.

Immunogène

neuropilin 2 recombinant protein epitope signature tag (PrEST)

Application

All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project and as a result, are supported by the most extensive characterization in the industry.

The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. We also provide Prestige Antibodies® protocols and other useful information.

Actions biochimiques/physiologiques

NRPs (neuropilins) mainly interact with vascular endothelial growth factor (VEGF) receptors, class 3 semaphorins and other receptors. Absence of NRP2 in mice shows mild phenotypic effects in lymphatic system development and axon guidance. NRP2 is also expressed in various cancers and is associated with the proliferation, survival and migration of cancer cells. NRP2 interaction with SEMA3F (semaphorin 3F) reduces PI-3K (phosphoinositide 3 kinase) activity, mTORC2 (mammalian target of rapamycin complex 2)-associated signaling, RhoA (Ras homolog gene family, member A) activity and suppresses the making of cytoskeletal stress fibers.

Caractéristiques et avantages

Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

Every Prestige Antibody is tested in the following ways:
  • IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
  • Protein array of 364 human recombinant protein fragments.

Liaison

Corresponding Antigen APREST78075

Forme physique

Solution in phosphate buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide.

Informations légales

Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany

Clause de non-responsabilité

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

USCAP 2022 Abstracts: Genitourinary Pathology (including renal tumors) (522-659).
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 35(Suppl 2), 657-806 (2022-03-19)
Concurrent Expression of VEGF-C and Neuropilin-2 Is Correlated with Poor Prognosis in Glioblastoma.
Zhao H, et al.
The Tohoku Journal of Experimental Medicine, 238, 85-91 (2016)
USCAP 2022 Abstracts: Genitourinary Pathology (including renal tumors) (522-659).
Laboratory investigation; a journal of technical methods and pathology, 102(Suppl 1), 583-732 (2022-03-19)
Evalynn Vasquez et al.
JCI insight, 2(3), e90617-e90617 (2017-02-15)
Chronic urethral obstruction and the ensuing bladder wall remodeling can lead to diminished bladder smooth muscle (BSM) contractility and debilitating lower urinary tract symptoms. No effective pharmacotherapy exists to restore BSM contractile function. Neuropilin 2 (Nrp2) is a transmembrane protein
Triggers for autism: genetic and environmental factors.
Matsuzaki H, et al.
Journal of Central Nervous System Disease, 4, 27-36 (2012)

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