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Cytokine IK Antibody

On Promotion

Catalog Number: orb214090

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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 Numberorb214090
CategoryAntibodies
DescriptionThe Cytokine IK Antibody is suitable for IHC, WB. It is a Polyclonal, Unconjugated antibody which raised against KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human Cytokine IK. The exact sequence is proprietary. Purification: The antibody was purified by immunogen affinity chromatography.
ClonalityPolyclonal
Species/HostRabbit
ConjugationUnconjugated
ReactivityBovine, Human, Monkey, 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.
ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human Cytokine IK. The exact sequence is proprietary.
UniProt IDQ13123, Q66HG8
Tested applicationsIHC, WB
Dilution rangeWB: 1-500-1-1000, IHC-P: 1-100-1-200, IP: 1-10-1-100
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 namesRED; RER; Protein Red; Cytokine IK; IK factor; Pro
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Research AreaEpigenetics, Infectious Diseases
NoteFor research use only
Entrez291659, 3550
Expiration Date12 months from date of receipt.
Images
Cytokine IK Antibody

Western blot analysis of Cytokine IK expression in mouse lung (A), mouse kidney (B) whole cell lysates. (Predicted band size: 65 kD; Observed band size: 66 kD)

Cytokine IK Antibody

Immunohistochemical analysis of Cytokine IK 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 (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.

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