PU.1 (SPI-1) (B-Cell Marker) (PU1/2146), CF647 conjugate, 0.1mg/mL, Clone: [PU1/2146], Mouse, Monoclonal

Artikelnummer: BOT-BNC472146-500
Artikelname: PU.1 (SPI-1) (B-Cell Marker) (PU1/2146), CF647 conjugate, 0.1mg/mL, Clone: [PU1/2146], Mouse, Monoclonal
Artikelnummer: BOT-BNC472146-500
Hersteller Artikelnummer: BNC472146-500
Alternativnummer: BOT-BNC472146-500-500UL
Hersteller: Biotium
Wirt: Mouse
Kategorie: Antikörper
Applikation: FC, IF, IHC, WB
Spezies Reaktivität: Human
Immunogen: Recombinant fragment (around aa 16-170) of human PU.1 protein (Exact sequence is proprietary)
Konjugation: CF647
Alternative Synonym: Transcription Factor spi1, 31kDa Transforming Protein, Hematopoietic Transcription Factor PU.1, SFPI1, SPI1, SPIA, Spleen focus forming virus (SFFV) proviral integration oncogene spi1
PU.1 is a member of the ETS family of transcription factors and is important for normal B-cell development. It is expressed in the myeloid lineage and in immature as well as mature B-lymphocytes, with the exception of plasma cells. PU.1 is expressed in germinal center B-cells and mantle B-cells. Various lymphomas are also positive for this marker. It is essential during early B-cell differentiation. The absence of PU.1 results in total block of B-cell development at the pre-pro stage. PU.1 plays a key role in normal myeloid differentiation, and regulates the expression of immunoglobulin and other genes that are important for B-cell development. 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: 0.1 mg/mL
Klon-Bezeichnung: [PU1/2146]
Molekulargewicht: 40 kDa
UniProt: P17947
Puffer: PBS, 0.1% 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): 1-2 ug/mL for 30 minutes at RT|Western Blot 0.5-1 ug/mL|Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM citrate buffer, pH 6.0, for 10-20 minutes followed by cooling at RT for 20 minutes|Optimal dilution for a specific application should be determined by user