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Anti-SF1 (Phospho-S82) Antibody

Catalog Number: orb393160

DispatchUsually dispatched within 5-10 working days
$ 160.00
Catalog Numberorb393160
CategoryAntibodies
DescriptionRabbit polyclonal antibody to SF1 (Phospho-S82)
TargetSF1
ClonalityPolyclonal
Species/HostRabbit
ConjugationUnconjugated
ReactivityHuman, Mouse, Rabbit, Rat, Zebrafish
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
PurificationThe antibody was purified by immunogen affinity chromatography.
ImmunogenKLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S82 of human SF1 protein. The exact sequence is proprietary.
UniProt IDQ15637, Q64213
Tested applicationsIF, IH, WB
Dilution rangeWB: 1:500:1000, IHC-P: 1:100:200, IF/ICC: 1:100:500
Antibody TypePrimary Antibody
SourceRabbit
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Alternative namesZFM1; ZNF162; Splicing factor 1; Mammalian branch
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NoteFor research use only
Entrez7536
Anti-SF1 (Phospho-S82) Antibody

Western blot analysis of SF1 (Phospho-S82) expression in SHSY5Y (A), Jurkat (B) whole cell lysates. (Predicted band size: 68 kD; Observed band size: 68 kD)

Anti-SF1 (Phospho-S82) Antibody

Immunohistochemical analysis of SF1 (Phospho-S82) staining in human breast cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (Phospho-H 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Anti-SF1 (Phospho-S82) Antibody

Immunofluorescent analysis of SF1 (Phospho-S82) staining in Jurkat cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark.