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Recombinant Rhesus macaque ICOS/AILIM/CD278 Protein (Fc Tag) | Elabscience Biotechnology
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Recombinant Rhesus macaque ICOS/AILIM/CD278 Protein (Fc Tag)

SKU: PKSQ050074-50

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Recombinant Rhesus macaque ICOS/AILIM/CD278 Protein (Fc Tag)

 

SKU # PKSQ050074
Expression Host HEK293 Cells

 

 

Description

Synonyms AILIM, CD278, CVID1, ICOS, Inducible T-cell costimulator, activation-inducible lymphocyte immunomediatory molecule
Species Rhesus macaque
Expression Host HEK293 Cells
Sequence Gly20-Lys140
Accession H9Z062
Calculated Molecular Weight 40.8 kDa
Observed Molecular Weight 50-60 kDa
Tag C-Fc
Bio-activity Not validated for activity
  

 

Properties

Purity > 90 % 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 a 0.2 μm filtered solution of 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 T-cell costimulator, also known as activation-inducible lymphocyte immunomediatory molecule, CD278, AILIM, CVID1 and ICOS, belongs to the CD28 and CTLA4 cell surface receptor family.. ICOS contains one Ig-like V-type domain and exsits as a homodimer with disulfide-linked. ICOS is highly expressed on tonsillar T-cellsand can be induced by PMA and ionomycin, ICOS plays an important role in cell-cell signaling, immune responses, and regulation of cell proliferation. Defects in ICOS are the cause of immunodeficiency common variable type 1, which is a primary immunodeficiency characterized by antibody deficiency, hypogammaglobulinemia, recurrent bacterial infections and an inability to mount an antibody response to antige.

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