CD29 (Stem Cell Marker)(12G10), 0.2mg/mL, Clone: [12G10], Mouse, Monoclonal

Artikelnummer: BOT-BNUB2905-100
Artikelname: CD29 (Stem Cell Marker)(12G10), 0.2mg/mL, Clone: [12G10], Mouse, Monoclonal
Artikelnummer: BOT-BNUB2905-100
Hersteller Artikelnummer: BNUB2905-100
Alternativnummer: BOT-BNUB2905-100-100UL
Hersteller: Biotium
Wirt: Mouse
Kategorie: Antikörper
Applikation: FC, Functional Studies, IF, IP
Spezies Reaktivität: Human
Immunogen: Purified human beta 1 integrin from HT1080 fibrosarcoma cell extract.
Alternative Synonym: Fibrinogen Receptor beta subunit, FNRB, Glycoprotein IIa (GPIIA), Integrin beta-1 (ITGB1), integrin VLA-4 beta subunit, MDF2, MSK12, Very Late Activation Protein beta Polypeptide, VLA-4 subunit beta, VLA-BETA, VLAB
Recognizes CD29. Binds to the cell membrane of T- and B- lymphocytes, monocytes, platelets, fibroblasts, endothelial cells, mast cells and smooth muscle cells. CD29 is an adhesion receptor and co-stimulatory molecule. This antigen was initially characterized as GPIIa on platelets and as the common b1 subunit of the very late antigen (VLA) protein family. CD29 forms a non-covalent heterodimeric complex with integrin alpha subunits. It also mediates adhesion to invasion and thrombospondin. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Klonalität: Monoclonal
Konzentration: 0.2 mg/mL
Klon-Bezeichnung: [12G10]
Molekulargewicht: 110 kDa (non-reduced) & 130 kDa (reduced)
UniProt: P05556
Puffer: PBS, 0.05% BSA, 0.05% azide
Quelle: Animal
Anwendungsbeschreibung: Does not react with Mouse or Rat, ELISA: For coating use Ab at 1-5 ug/mL, order Ab without BSA, Optimal dilution for a specific application should be determined by user.|Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody