Glucose Regulated Protein 94 (GRP94) (9G10.F8.2), 0.2mg/mL, Clone: [9G10.F8.2], Rat, Monoclonal

Artikelnummer: BOT-BNUB0940-500
Artikelname: Glucose Regulated Protein 94 (GRP94) (9G10.F8.2), 0.2mg/mL, Clone: [9G10.F8.2], Rat, Monoclonal
Artikelnummer: BOT-BNUB0940-500
Hersteller Artikelnummer: BNUB0940-500
Alternativnummer: BOT-BNUB0940-500-500UL
Hersteller: Biotium
Wirt: Rat
Kategorie: Antikörper
Applikation: FC, IF, IHC
Spezies Reaktivität: Bovine, Canine, Equine, Gallus, Guinea pig, Hamster, Human, Monkey, Mouse, Porcine, Rabbit, Rat, Sheep, Xenopus
Immunogen: Purified glucose regulated protein 94 (grp94) from chicken oviducts
Alternative Synonym: Glucose Regulated Protein 94, 94kDa glucose-regulated protein, Endoplasmin, Endothelial cell (HBMEC) glycoprotein (ECGP), Heat shock protein 90kDa beta member 1 (HSP90B1), Stress inducible tumor rejection antigen GP96, TRA1, Tumor rejection antigen-1 (gp96)
Recognizes a protein of 94 kDa, which is identified as the glucose-regulated protein 94 (grp94) and also tumor rejection antigen (gp96). Grp94 shows a high degree of sequence homology with the heat shock protein 90 (hsp90). This MAb is highly specific to grp94 and shows minimal cross-reaction with other members of the HSP90 family. Grp s are a class of proteins unresponsive to heat shock and are induced by glucose deprivation. Grp94 has been briefly studied as a prognostic factor in breast cancer.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: [9G10.F8.2]
Molekulargewicht: 94 kDa
UniProt: P14625
Puffer: PBS, 0.05% BSA, 0.05% azide
Quelle: Animal
Anwendungsbeschreibung: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunohistology (Formalin-fixed) 0.5-1.0 ug/mL|Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Immunofluorescence 0.5-1.0 ug/mL|Western blotting 0.5-1.0 ug/mL|Optimal dilution for a specific application should be determined by user