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Recombinant Mouse Integrin alpha V beta 8 Protein, CF  50 UG图1

Recombinant Mouse Integrin alpha V beta 8 Protein, CF 50 UG

2024-11-24 18:35IP属地 广东省东莞市 电信00留言

8314-AV

 

Formulation Lyophilized from a 0.2 μm filtered solution in PBS and Trehalose.


Reconstitution Reconstitute at 500 μg/mL in sterile PBS.



Shipping The product is shipped at ambient temperature. 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, 2 to 8 °C under sterile conditions after reconstitution.

  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.


Background: Integrin alpha V beta 8

Integrin  alpha V beta 8 is a type I transmembrane non-covalent heterodimer composed of a 115 kDa alpha V/CD51 subunit and an 84 kDa beta 8 subunit. The Integrin  beta 8 exclusively partners with the alpha V subunit, while alpha V forms heterodimers with beta 1, beta 3, beta 5 and beta 6 (1). Integrin  alpha V beta 8 is expressed on Schwann cells and astrocytes in the brain, vascular epithelial cells, mesangial cells in the kidney, and fibroblasts and epithelial cells in the airway (2-7). Interestingly, Integrin alpha V beta 8 is expressed by cells of the immune system, most prominently on CD4  + T cells and on dendritic cells (8). Unlike other alpha V integrins, alpha V beta 8 does not interact with the cytoskeleton or activate cytoplasmic signaling pathways (3, 9). Instead, it binds ligands containing an arginine-glycine-aspartic acid (RGD) motif, including Vitronectin, Fibrin and the latency associated peptide (LAP) (10, 11). High affinity binding of alpha V beta 8 to LAP triggers the MT1-MMP induced proteolytic cleavage of LAP and the release of active TGF-beta (12). Active TGF-beta regulates cell growth and nearby vascularization (5, 12, 13). Furthermore, Integrin alpha V beta 8-mediated TGF-beta activation in specialized dendritic cells of the intestine is crucial for maintaining immune homeostasis in the gut (14). Deletion of either alpha V or beta 8 reveals that alpha V beta 8 is required for vascular morphogenesis in the embryonic brain (15-16). The 958 amino acid mouse alpha V extracellular domain (ECD) shares 92% and 88% aa sequence identity with human and rat alpha V, respectively, while the 637 aa mouse beta 8 ECD shares 87% and 96% aa sequence identity with human and rat orthologs, respectively.

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