Anti-TP53INP1 抗体

• IHC-P

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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TP53INP1 antibody (AB9775)

Immunohistochemistry (Formalin-fixed paraffin embedded sections) of human liver tissue labelingp53 DINP1/TP53INP1 with Anti-p53 DINP1/TP53INP1 antibody (ab9775) at 5μg/ml.

• WB

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Western blot - Anti-TP53INP1 antibody (AB9775)

Western blot analysis of p53DINP1 expression in human lung tissue lysate with anti-p53DINP1 (ab9775) at 2 μg/ml in the absence (lane 1) or presence (lane 2) of blocking peptide (ab9776). Western blot analysis of p53DINP1 expression in human lung tissue lysate with anti-p53DINP1 (ab9775) at 2 µg/ml in the absence (lane 1) or presence (lane 2) of blocking peptide (ab9776).

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Western blot - Anti-TP53INP1 antibody (ab9775)

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• WB

CiteAb

Western blot - Anti-TP53INP1 antibody (AB9775)

TP53INP1 western blot using anti-TP53INP1 antibody ab9775. Publication image and figure legend from Jiang, F., Liu, T., et al., 2011, BMC Cancer, PubMed 21970405.

ab9775 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab9775 please see the product overview.

MiR-125b negatively regulated TP53INP1 protein levels in EC cells. A. Putative binding sites of miR-125b in the TP53INP1 3'UTR (white sequences) predicted by TargetScan. B. TP53INP1 protein levels were measured in EC cells at 72 h post-transfection by western blot assays. C. Potential binding site of miR-125b on TP53INP1 3'UTR in different species. The seed sequence is underlined. D. Sketch of the construction of pMIR-TP53INP1-3'UTR-WT or pMIR-TP53INP1-3'UTR-MT vectors. The mutant binding site is underlined and italicized. E. MiR-125bm down-regulated luciferase activities controlled by wild-type TP53INP1 3'UTR, but did not affect luciferase activity controlled by mutant TP53INP1 3'UTR (white sequences were mutated). The results are means of three independent experiments ± SD. (**P < 0.01 vs. blank; #P > 0.05 vs. blank).

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