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METTL7A Antibody

On Promotion

Catalog Number: orb341450

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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 Numberorb341450
CategoryAntibodies
DescriptionThe METTL7A Antibody is suitable for IF, IHC, WB. It is a Polyclonal, Unconjugated antibody which raised against Recombinant fusion protein of human METTL7A .Purification: The antibody was purified by immunogen affinity chromatography.
ClonalityPolyclonal
Species/HostRabbit
ConjugationUnconjugated
ReactivityHuman
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 METTL7A
UniProt IDQ9H8H3
Tested applicationsIF, IHC, WB
Dilution rangeWB: 1:500-1:2000, IHC-P: 1:50-1:200
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 namesMethyltransferase-like protein 7A; Protein AAM-B
NoteFor research use only
Entrez25840
Images
METTL7A Antibody

Western blot analysis of METTL7A expression in 22RV1 (A) whole cell lysates. (Predicted band size: 28 kD; Observed band size: 28 kD)

METTL7A Antibody

Immunohistochemical analysis of METTL7A staining in rat liver 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.

METTL7A Antibody

Immunofluorescent analysis of METTL7A staining in L929 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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