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TET1 Antibody

On Promotion

Catalog Number: orb412004

Select Product Size
SizePriceQuantity
30 μl$ 120.00
50 μl$ 160.00
100 μl$ 240.00
200 μl$ 340.00
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DispatchUsually dispatched within 5-10 working days
Product Properties
Catalog Numberorb412004
CategoryAntibodies
DescriptionThe TET1 Antibody is suitable for IF, IHC, IP, WB. It is a Polyclonal, Unconjugated antibody which raised against Recombinant fusion protein of human TET1 .Purification: The antibody was purified by immunogen affinity chromatography.
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 TET1
UniProt IDQ3URK3, Q8NFU7
Tested applicationsIF, IHC, IP, WB
Dilution rangeWB: 1:500-2000, IP: 1:50-100
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 namesCXXC6; KIAA1676; LCX; Methylcytosine dioxygenase T
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Research AreaEpigenetics
NoteFor research use only
Entrez80312, 52463
Images
TET1 Antibody

Western blot analysis of TET1 expression in A431 (A) whole cell lysates. (Predicted band size: 235 kD; Observed band size: 235 kD)

TET1 Antibody

Immunohistochemical analysis of TET1 staining in mouse testis 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.

TET1 Antibody

Immunofluorescent analysis of TET1 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 humidified chamber. Cells were washed with PBST and incubated with a AF594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

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