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LIF Antibody

Catalog Number: orb256655

Select Product Size
SizePriceQuantity
30 μl$ 120.00
50 μl$ 160.00
100 μl$ 240.00
200 μl$ 340.00
30 μl Enquire
50 μl Enquire
100 μl Enquire
200 μl Enquire
DispatchUsually dispatched within 5-10 working days
Catalog Numberorb256655
CategoryAntibodies
DescriptionRabbit polyclonal antibody to LIF
ClonalityPolyclonal
Species/HostRabbit
ConjugationUnconjugated
ReactivityBovine, Human, Mouse, Porcine, Rat, Sheep
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 LIF. The exact sequence is proprietary.
UniProt IDP15018, P17777, P09056
Tested applicationsIF, IHC, WB
Dilution rangeWB: 1:500-1000
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 namesHILDA; Leukemia inhibitory factor; LIF; Differenti
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Research AreaEpigenetics
NoteFor research use only
Entrez3976, 16878
Expiration Date12 months from date of receipt.
LIF Antibody

Western blot analysis of LIF expression in HCT116 (A), LO2 (B), mouse testis (C), rat testis (D) whole cell lysates. (Predicted band size: 22 kD; Observed band size: 24 kD)

LIF Antibody

Immunohistochemical analysis of LIF staining in human colon 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.

LIF Antibody

Immunofluorescent analysis of LIF staining in A549 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 AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).

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