Recombinant Human ICOS Ligand/ICOSL Protein (Fc Tag)
SKU: PKSH031086-100
Recombinant Human ICOS Ligand/ICOSL Protein (Fc Tag)
SKU # | PKSH031086 |
Expression Host | HEK293 Cells |
Description
Synonyms | B7 Homolog 2, B7-H2, B7-Like Protein Gl50, B7-Related Protein 1, B7H2, B7RP-1, B7RP1, CD275, ICOS Ligand, ICOSL, ICOSLG, KIAA0653 |
Species | Human |
Expression Host | HEK293 Cells |
Sequence | Met 1-Ser258 |
Accession | O75144-1 |
Calculated Molecular Weight | 53.7 kDa |
Observed Molecular Weight | 66-76&33 kDa |
Tag | C-hFc |
Bio-activity | Not validated for activity |
Properties
Purity | > 95 % as determined by reducing SDS-PAGE. |
Endotoxin | < 1.0 EU per μg of the protein as determined by the LAL method. |
Storage | Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months. |
Shipping | This product is provided as lyophilized powder which is shipped with ice packs. |
Formulation | Lyophilized from sterile PBS, pH 7.4 Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization. Please refer to the specific buffer information in the printed manual. |
Reconstitution | Please refer to the printed manual for detailed information. |
Background
Inducible co-stimulator ligand (ICOSL), also known as B7-H2, is a member of the B7 family of co-stimulatory molecules related to B7-1 and B7-2. It is a transmembrane glycoprotein with extracellular IgV and IgC domains, and binds to ICOS on activated T cells, thus delivers a positive costimulatory signal for optimal T cell function. The structural features of ICOSL are crucial for its costimulatory function. Present study shows that ICOSL displays a marked oligomerization potential, resembling more like B7-1 than B7-2. B7-H2-dependent signaling may play an active role in a proliferative response rather than in cytokine and chemokine production. The CD28/B7 and ICOS/B7-H2 pathways are both critical for costimulating T cell immune responses. Deficiency in either pathway results in defective T cell activation, cytokine production and germinal center formation.