Myeloid-Associated Differentiation Marker(MYADM/972), CF568 conjugate, 0.1mg/mL, IgG1, Clone: [MYADM/972], Mouse, Monoclonal

Catalog Number: BOT-BNC680972-500
Article Name: Myeloid-Associated Differentiation Marker(MYADM/972), CF568 conjugate, 0.1mg/mL, IgG1, Clone: [MYADM/972], Mouse, Monoclonal
Biozol Catalog Number: BOT-BNC680972-500
Supplier Catalog Number: BNC680972-500
Alternative Catalog Number: BOT-BNC680972-500-500UL
Manufacturer: Biotium
Host: Mouse
Category: Antikörper
Application: IHC
Species Reactivity: Human, Primate
Immunogen: Recombinant human MYADM protein
Conjugation: CF568
Alternative Names: MYADM, myeloid associated differentiation marker, Myeloid upregulated protein, Protein SB135
Recognizes a myeloid associated differentiation antigen in the cytoplasm of mature granulocytes. It shows no reactivity with any other cell type in human tissues. Markers of myeloid cells are useful in the identification of different levels of cellular differentiation. It reacts with early precursor and mature forms of human and monkey myeloid cells. This MAb is useful for the detection of myeloid leukemias and granulocytic sarcomas. It can be used as a marker of granulocytes in normal tissues or inflammatory processes.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.
Clonality: Monoclonal
Concentration: 0.1 mg/mL
Clone Designation: [MYADM/972]
Molecular Weight: Unknown
Isotype: IgG1
UniProt: Q96S97
Buffer: PBS, 0.1% BSA, 0.05% azide
Source: Animal
Application Notes: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunofluorescence: 1-2 ug/mL|Immunohistology formalin-fixed 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 min followed by cooling at RT for 20 minutes|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Optimal dilution for a specific application should be determined by user