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Lamin A/C (Phospho-S22) Antibody

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Catalog Number: orb665684

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SizePriceQuantity
30 μl$ 140.00
50 μl$ 180.00
100 μl$ 280.00
200 μl$ 400.00
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DispatchUsually dispatched within 5-10 working days
Product Properties
Catalog Numberorb665684
CategoryAntibodies
DescriptionThe Lamin A/C (Phospho-S22) Antibody is suitable for IHC, WB. It is a Polyclonal, Unconjugated antibody which raised against KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S22 of human Lamin A/C protein. The exact sequence is proprietary. Purification: The antibody was purified by immunogen affinity chromatography.
ClonalityPolyclonal
Species/HostRabbit
ConjugationUnconjugated
ReactivityBovine, Human, Monkey, Mouse, Porcine, 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.
ImmunogenKLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S22 of human Lamin A/C protein. The exact sequence is proprietary.
UniProt IDP48679, P48678, P02545
Tested applicationsIHC, WB
Dilution rangeWB: 1-500-1000, IHC-P: 1-50-200
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 namesLMN1; Prelamin-A/C
Research AreaCardiovascular Disease, Epigenetics, Neuroscience
NoteFor research use only
Entrez16905, 4000, 60374
Images
Lamin A/C (Phospho-S22) Antibody

Western blot analysis of Lamin A/C (Phospho-S22) expression in A375 (A) whole cell lysates. (Predicted band size: 74 kD; Observed band size: 78; 69 kD)

Lamin A/C (Phospho-S22) Antibody

Immunohistochemical analysis of Lamin A/C (Phospho-S22) staining in human lymph node 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.

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