Human Junctional Adhesion Molecule 2 (JAM2) Protein

Este producto es parte de JAM - junctional adhesion molecule
Product Graph
234€ (2 µg)

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935106861
info@markelab.com
name
Human Junctional Adhesion Molecule 2 (JAM2) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx680075
tested applications
SDS-PAGE

Description

Human Junctional Adhesion Molecule 2 (JAM2) Protein is a recombinant protein produced in Sf9, Baculovirus cells.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryProteins and Peptides
Immunogen TargetJunctional Adhesion Molecule 2 (JAM2)
HostInsect
OriginHuman
ConjugationUnconjugated
ExpressionRecombinant
Purity> 90% (SDS-PAGE)
Size 12 µg
Size 210 µg
Size 31 mg
FormLiquid
Tested ApplicationsSDS-PAGE
AvailabilityShipped within 5-10 working days.
Dry IceNo
AliasJAMB,CD322,IBGC8,JAM-B,VEJAM,PRO245,VE-JAM,C21orf43,Vascular endothelial junction-associated molecule,Junctional adhesion molecule B
BackgroundProtein JAM2
StatusRUO
NoteThis product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

JAM2 is a member of the Junctional Adhesion Molecule (JAM) family, part of the immunoglobulin superfamily, and is primarily expressed in endothelial cells, lymphatic vessels, and certain immune cells. Structurally, JAM2 consists of two extracellular Ig-like domains, a single transmembrane domain, and a short cytoplasmic tail that interacts with intracellular signaling molecules and the actin cytoskeleton. JAM2 is involved in cell-cell adhesion, particularly in maintaining endothelial barrier integrity and regulating the movement of immune cells through endothelial junctions. It plays a role in leukocyte transmigration during inflammation and immune surveillance by interacting with integrins, including α4β1 integrin on leukocytes. JAM2 also mediates vascular permeability and contributes to the organization of tight junctions between endothelial and epithelial cells. JAM2 is implicated in pathological processes such as inflammatory diseases, autoimmunity, and cancer metastasis, where it regulates the extravasation of leukocytes and cancer cells. Dysregulation of JAM2 has been linked to abnormal vascular permeability and inflammatory responses, making it a potential therapeutic target in conditions like vascular inflammation and tumor progression.

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