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Anti-c-Myc (Phospho-T358) Antibody

Catalog Number: orb315625

DispatchUsually dispatched within 5-10 working days
$ 160.00
Catalog Numberorb315625
CategoryAntibodies
DescriptionRabbit polyclonal antibody to c-Myc (Phospho-T358)
Species/HostRabbit
ClonalityPolyclonal
Tested applicationsIF, IH, IP, WB
ReactivityHuman
ImmunogenKLH-conjugated synthetic phosphopeptide corresponding to residues surrounding T358 of human c-Myc protein. The exact sequence is proprietary.
Antibody TypePrimary Antibody
Dilution rangeWB: 1-500:1000, IHC-P: 1-100:200, IF/ICC: 1-100:500, IP: 1-10:100
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
ConjugationUnconjugated
TargetMYC
Entrez4609
UniProt IDP01106
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.
Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Alternative namesanti BHLHE39 antibody, anti Myc proto-oncogene pro
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NoteFor research use only
Expiration Date12 months from date of receipt.
Anti-c-Myc (Phospho-T358) Antibody

Western blot analysis of c-Myc (Phospho-T358) expression in Hela (A), HEK293T EGF-treated (B), A431 (C) whole cell lysates. (Predicted band size: 48 kD; Observed band size: 57 kD)

Anti-c-Myc (Phospho-T358) Antibody

Immunohistochemical analysis of c-Myc (Phospho-T358) 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-c-Myc (Phospho-T358) Antibody

Immunofluorescent analysis of c-Myc (Phospho-T358) staining in HeLa 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.