![Western Blot: DNA-PKcs Antibody [NB100-658] - MDA-MB-231, MCF-7, SUM149, SUM159, T47D, HCC1954 whole cell lysates (50 ug/lane). 10% SDS-PAGE. DNA-PKcs (NB100-658) primary antibody at 1:1000, 4C, overnight. Western blot image submitted by a verified customer review.](http://images.novusbio.com/fullsize/DNA-PKcs-Antibody-Western-Blot-NB100-658-img0025.jpg "Western Blot: DNA-PKcs Antibody [NB100-658] - MDA-MB-231, MCF-7, SUM149, SUM159, T47D, HCC1954 whole cell lysates (50 ug/lane). 10% SDS-PAGE. DNA-PKcs (NB100-658) primary antibody at 1:1000, 4C, overnight. Western blot image submitted by a verified customer review.")
| Reactivity | HuSpecies Glossary |
| Applications | WB, IP, KD |
| Clonality | Polyclonal |
| Host | Rabbit |
| Conjugate | Unconjugated |
| Concentration | 0.2 mg/ml |
| Immunogen | The immunogen recognized by this antibody maps to a region between residues 2050 and 2100 of human DNA-Dependent Protein Kinase, catalytic subunit using the numbering given in entry NP_008835.5 (GeneID 5591). |
| Isotype | IgG |
| Clonality | Polyclonal |
| Host | Rabbit |
| Gene | PRKDC |
| Purity | Immunogen affinity purified |
| Innovator's Reward | Test in a species/application not listed above to receive a full credit towards a future purchase. |
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| Application Notes | Ku-80 co-immunoprecipitates with DNA-PKcs when using this antibody. DNA-PKcs antibody is validated for WB from a verified customer review. |
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| Storage | Store at 4C. Do not freeze. |
| Buffer | TBS, 0.1% BSA |
| Preservative | 0.09% Sodium Azide |
| Concentration | 0.2 mg/ml |
| Purity | Immunogen affinity purified |
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| Images | Ratings | Applications | Species | Date | Details | ||||||||||
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Enlarge |
reviewed by:
Yongkang Yang |
WB | Human | 08/16/2019 |
Summary
Comments
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Secondary Antibodies |
Isotype Controls |
Research Areas for DNA-PKcs Antibody (NB100-658)Find related products by research area.
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![Western Blot: DNA-PKcs Antibody [NB100-658] - Detection of Human DNA-PKcs in HeLa whole cell lystate using NB100-658. DNA-PKcs was also immunoprecipitated using rabbit anti-DNA-PKcs antibodies NB100-657, NB100-659 and NB100-660.](http://images.novusbio.com/fullsize/DNA-PKcs-Antibody-Western-Blot-NB100-658-img0023.jpg "Western Blot: DNA-PKcs Antibody [NB100-658] - Detection of Human DNA-PKcs in HeLa whole cell lystate using NB100-658. DNA-PKcs was also immunoprecipitated using rabbit anti-DNA-PKcs antibodies NB100-657, NB100-659 and NB100-660.")
![Western Blot: DNA-PKcs Antibody [NB100-658] - Hep3B human hepatocellular carcinoma cell line. 50 ug cell lysate per lane. 10% SDS-PAGE. DNA-PKcs antibody at 1:1000 dilution O/N. Secondary antibody: HRP-conjugated Donkey anti-rabbit IgG polyclonal antibody at 1:2000 dilution. WB image submitted by a verified customer review.](http://images.novusbio.com/fullsize/DNA-PKcs-Antibody-Western-Blot-NB100-658-img0024.jpg "Western Blot: DNA-PKcs Antibody [NB100-658] - Hep3B human hepatocellular carcinoma cell line. 50 ug cell lysate per lane. 10% SDS-PAGE. DNA-PKcs antibody at 1:1000 dilution O/N. Secondary antibody: HRP-conjugated Donkey anti-rabbit IgG polyclonal antibody at 1:2000 dilution. WB image submitted by a verified customer review.")
![Knockdown Validated: DNA-PKcs Antibody [NB100-658] - Molecular Characterization of G1 Resection. End joining events in GC92 cells treated with siKu70/80, siLig4, siLig1/3, or DNA-PKcs antibody. Data are mean +/- SEM. Image collected and cropped by CiteAb from the following publication (//www.ncbi.nlm.nih.gov/pmc/articles/PMC5316416/) licensed under a CC-BY license.](http://images.novusbio.com/fullsize/DNA-PKcs-Antibody-Knockdown-Validated-NB100-658-img0026.jpg "Knockdown Validated: DNA-PKcs Antibody [NB100-658] - Molecular Characterization of G1 Resection. End joining events in GC92 cells treated with siKu70/80, siLig4, siLig1/3, or DNA-PKcs antibody. Data are mean +/- SEM. Image collected and cropped by CiteAb from the following publication (//www.ncbi.nlm.nih.gov/pmc/articles/PMC5316416/) licensed under a CC-BY license.")
![Western Blot: DNA-PKcs Antibody [NB100-658] - Molecular Characterization of G1 Resection(A) Schematic of the NHEJ reporter assay. The repair of two I-SceI-induced DSBs can result in loss of the intervening fragment, which is detected by a CD4+ signal (Rass et al., 2009). CD4+ clones were amplified by PCR (green arrows) across the repair site & sequenced. Repair of the two DSBs can also occur without loss of the intervening fragment, which escapes detection.(B) gamma H2AX foci in GC92 WT & Artemis KO cells treated with siDNA-PKcs or siCtIP. Cells were transfected with I-SceI, & foci were scored in I-SceI+ & I-SceI− cells (identified by immunofluorescence [IF] against I-SceI). Data are mean ± SEM.(C) End joining events in GC92 WT & Artemis KO cells containing the NHEJ reporter substrate. Cells were transfected with RFP or cMyc-Artemis constructs. Events were quantified by the fraction of CD4+ & RFP/cMyc+cells relative to all RFP/cMyc+cells, & results were normalized to WT cells. Data are mean ± SEM.(D) End joining events in GC92 WT & Artemis KO cells treated with siCtIP. Data are mean ± SEM.(E) Distribution of deletion sizes obtained from the sequence analysis of GC92 WT & siLig1/3-treated cells. nt, nucleotide.(F) End joining events in GC92 cells treated with siKu70/80, siLig4, siLig1/3, or siDNA-PKcs. Data are mean ± SEM.See also Table S1. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/28132842), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nb100-658_rabbit-polyclonal-dna-pkcs-antibody-31020241682113.jpg "Western Blot: DNA-PKcs Antibody [NB100-658] - Molecular Characterization of G1 Resection(A) Schematic of the NHEJ reporter assay. The repair of two I-SceI-induced DSBs can result in loss of the intervening fragment, which is detected by a CD4+ signal (Rass et al., 2009). CD4+ clones were amplified by PCR (green arrows) across the repair site & sequenced. Repair of the two DSBs can also occur without loss of the intervening fragment, which escapes detection.(B) gamma H2AX foci in GC92 WT & Artemis KO cells treated with siDNA-PKcs or siCtIP. Cells were transfected with I-SceI, & foci were scored in I-SceI+ & I-SceI− cells (identified by immunofluorescence [IF] against I-SceI). Data are mean ± SEM.(C) End joining events in GC92 WT & Artemis KO cells containing the NHEJ reporter substrate. Cells were transfected with RFP or cMyc-Artemis constructs. Events were quantified by the fraction of CD4+ & RFP/cMyc+cells relative to all RFP/cMyc+cells, & results were normalized to WT cells. Data are mean ± SEM.(D) End joining events in GC92 WT & Artemis KO cells treated with siCtIP. Data are mean ± SEM.(E) Distribution of deletion sizes obtained from the sequence analysis of GC92 WT & siLig1/3-treated cells. nt, nucleotide.(F) End joining events in GC92 cells treated with siKu70/80, siLig4, siLig1/3, or siDNA-PKcs. Data are mean ± SEM.See also Table S1. Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/28132842), licensed under a CC-BY license. Not internally tested by Novus Biologicals.")
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