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OGT Antibody

Catalog Number: orb340807

Select Product Size
SizePriceQuantity
30 μl$ 120.00
50 μl$ 160.00
100 μl$ 240.00
200 μl$ 340.00
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50 μl Enquire
100 μl Enquire
200 μl Enquire
DispatchUsually dispatched within 5-10 working days
Catalog Numberorb340807
CategoryAntibodies
DescriptionRabbit polyclonal antibody to OGT
ClonalityPolyclonal
Species/HostRabbit
ConjugationUnconjugated
ReactivityHuman, Mouse, Rat
Form/AppearanceLiquid 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.
ImmunogenRecombinant fusion protein of human OGT
UniProt IDO15294, Q8CGY8, P56558
Tested applicationsIF, IHC, IP, WB
Dilution rangeWB: 1:500-1:2000, IHC-P: 1:50-1:200, IF/ICC: 1:50-1:200, IP: 1:20-1:50
Antibody TypePrimary Antibody
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 namesUDP-N-acetylglucosamine--peptide N-acetylglucosami
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Research AreaApoptotic, Cancer, Epigenetics, Infectious Disease
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NoteFor research use only
Entrez108155, 8473, 26295
Expiration Date12 months from date of receipt.
OGT Antibody

Western blot analysis of OGT expression in K562 (A), A549 (B), Hela (C), mouse spleen (D), mouse brain (E) whole cell lysates. (Predicted band size: 74; 103; 115; 116 kD; Observed band size: 117 kD)

OGT Antibody

Immunohistochemical analysis of OGT staining in rat heart formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 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.

OGT Antibody

Immunofluorescent analysis of OGT staining in U2OS 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.

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