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cd 102

" in TargetMol Product Catalog
  • Recombinant Protein
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ICAM-2/CD102 Protein, Mouse, Recombinant (hFc)
intercellular adhesion molecule 2,Ly-60,CD102,Icam-2
TMPY-01799
ICAM-2 CD102 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 50 kDa and the accession number is P35330.
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7-10 days
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ICAM-2/CD102 Protein, Mouse, Recombinant
Icam-2,intercellular adhesion molecule 2,Ly-60,CD102
TMPY-03533
ICAM-2 CD102 Protein, Mouse, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 23.6 kDa and the accession number is P35330.
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7-10 days
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ICAM-2/CD102 Protein, Human, Recombinant (His & hFc)
CD102,intercellular adhesion molecule 2
TMPY-00826
ICAM-2 CD102 Protein, Human, Recombinant (His & hFc) is expressed in HEK293 mammalian cells with His and hFc tag. The predicted molecular weight is 50.3 kDa and the accession number is P13598.
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7-10 days
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ICAM-2/CD102 Protein, Human, Recombinant (His)
CD102,intercellular adhesion molecule 2
TMPY-01418
ICAM-2 CD102 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 24 kDa and the accession number is P13598.
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7-10 days
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SLAMF2 Protein, Human, Recombinant (hFc & His)
Leukocyte antigen MEM-102,CD48 antigen,CD48,BCM1 surface antigen,B-lymphocyte activation marker BLAST-1,BLAST1,TCT.1,BCM1
TMPJ-00130
CD48 antigen, also known as B-lymphocyte activation marker BLAST-1, BCM1 surface antigen, Leukocyte antigen MEM-102, TCT.1, CD48, BCM1,and BLAST1, CD48 contains one Ig-like C2-type domain and one Ig-like V-type domain, but does not have a transmembrane domain, however, but is held at the cell surface by a GPI anchor via a C-terminal domain which maybe cleaved to yield a soluble form of the receptor. CD48 may facilitate interaction between activated lymphocytes and be involved in regulating T-cell activation. CD48 plays a vital role as an environmental sensor for regulating progenitor cell numbers and inhibiting tumor development. It is suggested that the anti-CD48 mAb has the potential to become an effective therapeutic mAb against multiple myeloma.
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7-10 days
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