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JAM2 belongs to the immunoglobulin superfamily, and the junctional adhesion molecule (JAM) family. Zusätzlich bieten wir Ihnen Junctional Adhesion Molecule 2 Antikörper (148) und Junctional Adhesion Molecule 2 Kits (10) und viele weitere Produktgruppen zu diesem Protein an.
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The developmental expression pattern of jam-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 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 expressed by neighbouring cells is essential for fusion.
JAM-B/JAM-C mediated interaction between endothelial cells and stellate cells stabilizes vessel walls and may control the sinusoidal diameter.
JAM-B is an as yet underappreciated trophoblast lineage-specific protein, which is modulated via the progesterone receptor and shows unique strain-specific kinetics.
identify neuronal junction adhesion molecule 2 (JAM2) as an inhibitory myelin-guidance molecule.
JAM-B expression was detected in de novo-formed blood vessels of tumors.
TGF-beta3 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 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) 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.
promotes lymphocyte transendothelial migration
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
IL-1alpha and TGF-beta2 regulate JAM-B expression in an opposite manner in sertoli cells.
this review briefly focuses on what is currently known about the structure, function, and mechanism of JAM-B, with particular emphasis on cancer. [review]
JAM-2 may function as a putative tumour suppressor in the progression and metastasis of colorectal cancer
This study showed thatJAM2 (rs2829841; intronic), associated with Alzheimer disease.
These data brought new evidences for the role of JAM2 and JAM3 in progression of gastric adenocarcinoma
role as an adhesive ligand for interacting with a variety of immune cell types
Discovery as ligand for the integrin alpha4beta1
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.
Cloning and discovery as adhesion receptor for T cells
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