S100A4 (Marker of Tumor Metastasis) (S100A4/1482), 0.2mg/mL, Clone: [S100A4/1482], Mouse, Monoclonal

Catalog Number: BOT-BNUB1482-500
Article Name: S100A4 (Marker of Tumor Metastasis) (S100A4/1482), 0.2mg/mL, Clone: [S100A4/1482], Mouse, Monoclonal
Biozol Catalog Number: BOT-BNUB1482-500
Supplier Catalog Number: BNUB1482-500
Alternative Catalog Number: BOT-BNUB1482-500-500UL
Manufacturer: Biotium
Host: Mouse
Category: Antikörper
Application: FC, IF, IHC, WB
Species Reactivity: Human, Mouse
Immunogen: Recombinant human S100A4 protein
Alternative Names: 18A2|42A|CAPL|Malignant transformation suppression 1 (MTS1)|Metastasin|P9KA|PEL98|Placental calcium-binding protein|S100 calcium-binding protein A4|S100A4
S100A4 belongs to the S100 super-family of proteins containing 2 EF-hand calcium-binding domains. S100 genes include at least 25 members, including S100A1-S100A18, trichohyalin, filaggrin, repetin, S100P, and S100Z. S100A4 exerts its function via direct interaction with a number of proteins including P53, P63, non-muscle myosin IIA, i6i4 integrin, and liprin b1. S100A4 is overexpressed in highly metastatic cancers, which makes it useful as a marker of tumor progression. 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: 0.2 mg/mL
Clone Designation: [S100A4/1482]
Molecular Weight: 10-12 kDa
UniProt: P26447
Buffer: PBS, 0.05% 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): 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 min|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Western blotting 0.5-1 ug/mL|Optimal dilution for a specific application should be determined by user