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Rockland Immunochemicals
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Bio-Rad
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ABclonal Biotechnology
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Merck KGaA
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Rabbit Anti Human MDC1 Polyclonal Affinity Purified (PBS with 0.02% sodium azide, 50% glycerol, pH7.3) (IHC,Immunofluorescence) from Innovative Research is a polyclonal antibody in a liquid format, buffered in PBS with 0.02% sodium azide, 50%
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The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to
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Sheep Anti-Human MDC1 (aa 1883-2089)
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Boster Bio Anti-MDC1 Monoclonal Antibody catalog # M01252. Tested in IF, ICC, WB applications. This antibody reacts with Human, Mouse.
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Boster Bio Anti-MDC1 Antibody catalog # A01252. Tested in WB,IHC,ICC/IF applications. This antibody reacts with Human.
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Rabbit anti-Human Phospho-MDC1 Polyclonal Antibody
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Image Search Results
Journal: Frontiers in Pharmacology
Article Title: NUP155 and NDC1 interaction in NSCLC: a promising target for tumor progression
doi: 10.3389/fphar.2024.1514367
Figure Lengend Snippet: Examines the role of NUP155 in cancer cells. (A) The intersection of NUP family and differentially expressed genes yielded 21 differentially expressed genes. NUP62CL.1 and POM121L2.1 were duplicated with NUP62CL and POM121L2. (B) Survival analysis of NDC1. (C) Survival analysis of NUP155. (D) NUP155 was knocked down, and Western blot was used to detect the protein expression changes of NUP155 and NDC1. (E) Histogram was used to show the Western blot results of NUP155 and NDC1. (F) Protein expression changes of NUP155 and NDC1 in cancer cells were detected after overexpression of NUP155. (G) Histogram was utilized to display the Western blot results of NUP155 and NDC1. (H) After NDC1 knockdown, the protein expression changes of NDC1 and NUP155 in cancer cells were detected. (I) Histogram was used to show the results of NUP155 and NDC1.
Article Snippet: Primary antibody information was listed as follow: NUP155 (1:1,000, Cat No. 66359-1-Ig, Proteintech, United States),
Techniques: Western Blot, Expressing, Over Expression, Knockdown
Journal: Frontiers in Pharmacology
Article Title: NUP155 and NDC1 interaction in NSCLC: a promising target for tumor progression
doi: 10.3389/fphar.2024.1514367
Figure Lengend Snippet: Growth changes of cancer cells were detected by experiments after the NDC1 expression changing. (A) The results of CCK-8 assay indicated that the viability of cancer cells was weakened after inhibition of NDC1. (B) After overexpression of NDC1, the results of CCK-8 assay showed that cancer cell viability was enhanced. (C) After NDC1 knockdown, the results of clone formation experiments showed that the migration ability of cancer cells had reduced. (D) After overexpression of NDC1, the results of Clone formation experiment confirmed that the migration ability of cancer cells was improved. (E) After NDC1 knockdown, the results of transwell assay showed that the invasion ability of cancer cells was weakened. (F) After overexpression of NDC1, the results of transwell assay confirmed that the invasion ability of cancer cells had enhanced. (G) After inhibition of NDC1, the expression of E-cadherin protein in cancer cells was enhanced, and the protein expression of Vimentin was weakened. After overexpression of NDC1, the expression of E-cadherin protein in cancer cells was decreased, and the protein expression of Vimentin was increased. (H) Histogram was used to show the results of E-cadherin and Vimentin in A549 cells.
Article Snippet: Primary antibody information was listed as follow: NUP155 (1:1,000, Cat No. 66359-1-Ig, Proteintech, United States),
Techniques: Expressing, CCK-8 Assay, Inhibition, Over Expression, Knockdown, Migration, Transwell Assay