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Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. Additionally we are shipping Junctional Adhesion Molecule 2 Antibodies (122) and Junctional Adhesion Molecule 2 Proteins (23) and many more products for this protein.
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The developmental expression pattern of jam (show F11R ELISA Kits)-b2 suggests that it may contribute different properties to extraocular muscles, jaw muscles, and pectoral fins.
results indicate that Jam1a-Jam2a interactions facilitate the transduction of requisite Notch (show NOTCH1 ELISA Kits) signals from the somite to the precursors of HSCs, and that these events occur well before formation of the dorsal aorta
interaction between Jamb and Jamc (show JAM3 ELISA Kits) expressed by neighbouring cells is essential for fusion.
JAM-B expression was detected in de novo-formed blood vessels of tumors.
TGF-beta3 (show TGFB3 ELISA Kits) significantly downregulates JAM-B expression via post-transcriptional and post-translational modulation and results in the disruption of BTB and apical ES.
Function of Jam-B/Jam-C (show JAM3 ELISA Kits) interaction in homing and mobilization of human and mouse hematopoietic stem and progenitor cells.
Data show that junctional adhesion molecule-B (JAM-B) expressed by endothelial cells contributes to murine B16 melanoma cells metastasis through its interaction with junctional adhesion molecule-C (JAM-C (show JAM3 ELISA Kits)) on tumor cells.
Jam2 has a role in the interaction between hatched blastocyst and receptive uterus.
JAM-B is an active player in the maintenance of the bone marrow stromal microenvironment.
Results suggest a role for junctional adhesion molecule-2 (JAM-2) in facilitating transmigration in endothelial cells.
Interactions with JAM-B and -C are essential for development of cutaneous inflammation.
These results demonstrate that Jam-B is dispensable for normal mouse development and stem cell identity in embryonic, neural, and hematopoietic stem cells.
JAM-B identifies a unique population of RGCs in which structure corresponds remarkably to function
JAM-2 may function as a putative tumour suppressor in the progression and metastasis of colorectal cancer
These data brought new evidences for the role of JAM2 and JAM3 (show JAM3 ELISA Kits) in progression of gastric adenocarcinoma
Results suggest a role for junctional adhesion molecule-2 (JAM-2) in facilitating transmigration in endothelial cells
Examine JAM-2 expression in normal/inflammed lymphatic endothelium.
This gene belongs to the immunoglobulin superfamily, and the junctional adhesion molecule (JAM) family. The protein encoded by this gene is a type I membrane protein that is localized at the tight junctions of both epithelial and endothelial cells. It acts as an adhesive ligand for interacting with a variety of immune cell types, and may play a role in lymphocyte homing to secondary lymphoid organs. Alternatively spliced transcript variants have been found for this gene.
junctional adhesion molecule B
, junctional adhesion molecule 2
, junction adhesion molecule B
, junction cell adhesion molecule 2
, vascular endothelial junction-associated molecule
, junction adhesion molecule 2