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    Abbr.:   ICAM2(Human)
         Source:  Mammalian Cells

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    Abbr.:   ICAM2, Fc-His(Human)
         Source:  Human Cells

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   Others >> Icam2(Mouse)

   Recombinant Mouse Intercellular Adhesion Molecule 2   [ Back  ]                         Price Inquiry

Cat. No.

Icam2-1746M

Description

Intercellular adhesion molecule 2 (ICAM2), also known as CD102 (Cluster of Differentiation 102), is a member of the intercellular adhesion molecule (ICAM) family. All ICAM proteins are type I transmembrane glycoproteins that bind to the leukocyte adhesion LFA-1 protein. This protein may play a role in lymphocyte recirculation by blocking LFA-1-dependent cell adhesion. It mediates adhesive interactions important for antigen-specific immune response, NK-cell mediated clearance, lymphocyte recirculation, and other cellular interactions important for immune response and surveillance.

Molecular Weight

The predicted molecular weight of Recombinant Mouse ICAM-2 is Mr 49.5 kDa. However, the actual molecular weight as observed by migration on SDS Page is Mr 75-80 kDa.

Source

NSO Cells.

State Of Matter

Lyophilized.

Purity

>95% by SDS Page and analyzed by silver stain.

Endotoxin

<1.0 EU/µg as determined by the LAL method.

Storage And Stability

This lyophilized protein is stable for six to twelve months when stored desiccated at -20 to -70. After aseptic reconstitution, this protein may be stored at 2 to 8 for one month or at -20 to -70 in a manual defrost freezer. Avoid Repeated Freeze Thaw Cycles. See Product Insert for exact lot specific storage instructions.

Gene Information

 

Gene Name

Icam2 intercellular adhesion molecule 2 [ Mus musculus ]

Synonyms

Icam2; intercellular adhesion molecule 2; CD102; Ly-60; Icam-2; OTTMUSP00000003460; OTTMUSP00000003463

GeneID

15896

mRNA Refseq

NM_010494

Protein Refseq

NP_034624

UniProt ID

P35330

Chromosome Location

11 E1; 11 63.0 cM

Pathway

Cell adhesion molecules (CAMs); Natural killer cell mediated cytotoxicity

Function

protein binding


PDB rendering based on 1zxq.

 

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