Disease and disorder research has been conducted in relation to the Interstrand Cross-link Repair Pathway and Fanconi Anemia, Anemia, Malignant Neoplasms, Neoplasms, Cytogenetic Abnormality. The study of the Interstrand Cross-link Repair Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Interstrand Cross-link Repair Pathway has been researched in relation to Dna Repair, Hypersensitivity, Cell Cycle, Dna Replication, Aging. The Interstrand Cross-link Repair Pathway complements our catalog of research reagents including antibodies and ELISA kits against FANCD2, ERCC1, DCLRE1A, FANCA, PCNA.
Interstrand Cross-link Repair Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Interstrand Cross-link Repair below!
For more information on how to use Laverne, please read the How to Guide.
We have 970 products for the study of the Interstrand Cross-link Repair Pathway that can be applied to Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: MTMR15 Antibody [H00022909-B01P] - Analysis of KIAA1018 expression in human spleen.](http://images.novusbio.com/fullsize2/MTMR15-Antibody-Western-Blot-H00022909-B01P-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: MTMR15 Antibody [H00022909-B01P] - Analysis of purified antibody to MTMR15 on HeLa cell. (antibody concentration 10 ug/ml)](http://images.novusbio.com/fullsize2/MTMR15-Antibody-Immunocytochemistry-Immunofluorescence-H00022909-B01P-img0003.jpg)
![Knockdown Validated: FANCD2 Antibody [NB100-182] - Effects of FANCD2 knockdown on levels of cell cycle regulators. Caki-1 cells were transfected with control siRNA (siCon) or FANCD2 siRNA (siFD2#2) and treated with AICAR for 24 h. The levels of FANCD2, p15Ink4B, and p21Cip1 were evaluated by immunoblotting. Image collected and cropped by CiteAb from the following publication (http://doi.wiley.com/10.1002/2211-5463.12185) licensed under a CC-BY licence.](http://images.novusbio.com/fullsize2/FANCD2-Antibody-Knockdown-Validated-NB100-182-img0040.jpg)
![Knockdown Validated: FANCD2 Antibody [NB100-182] - Resistance of FANCA-mutant cells with defective FANCD2 function to hydrogen peroxide (H2O2). Representative images illustrating staining for subnuclear FANCD2 foci in isogenic fibroblast pairs, either deficient for FANCD2 (PD20) or FANCA (PD220) and their respective wild-type (wt) complemented counterparts. Foci were visualized three hours after treatment with H2O2 (25 uM for 2 hours). Image collected and cropped by CiteAb from the following publication (http://www.hindawi.com/journals/bmri/2008/821529/) licensed under a CC-BY licence.](http://images.novusbio.com/fullsize2/FANCD2-Antibody-Knockdown-Validated-NB100-182-img0035.jpg)
![Immunohistochemistry-Paraffin: ERCC1 Antibody (8F1) [NB500-704] - Cyto-histologic comparison of anti-ERCC1 immunoreactivity using the protocol 8F1 CC1-mono (top) or 8F1 H2-60 (bottom). Left: Pleural effusion sediment of lung adenocarcinoma. Right: thoracic lymph node. Arrow: Lymphocyte. Arrowhead: Streak of endothelial cells. Asterisk: Tumor cell cluster. 400 A- original magnification. Image collected and cropped by Citeab from the following publication (Automated ERCC1 immunochemistry on hybrid cytology/tissue microarray of malignant effusions: evaluation of antibodies 8F1 and D-10. <i>J Clin Bioinforma</i> (2011) licensed under a CC-BY licence.](http://images.novusbio.com/fullsize2/ERCC1-Antibody-(8F1)-Immunohistochemistry-Paraffin-NB500-704-img0004.jpg)
![Immunohistochemistry-Paraffin: ERCC1 Antibody (8F1) [NB500-704] - Analysis of ERCC1 in human non-small cell lung cancer. Image courtesy of product review submitted by Alex Soltermann.](http://images.novusbio.com/fullsize2/ERCC1-Antibody-(8F1)-Immunohistochemistry-Paraffin-NB500-704-img0002.jpg)
![Western Blot: BRIP1/FANCJ Antibody [NBP1-31883] - Whole cell extract (30 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with FANCJ antibody [N1N2], N-term diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize2/BRIP1-FANCJ-Antibody-Western-Blot-NBP1-31883-img0017.jpg)
![Immunocytochemistry/Immunofluorescence: BRIP1/FANCJ Antibody [NBP1-31883] - 293T cells were fixed in 2% paraformaldehyde/culture medium at 37 degrees C for 30 min. Green: BRIP1 protein stained by FANCJ antibody [N1N2], N-term diluted at 1:500. Blue: Hoechst 33343 staining.](http://images.novusbio.com/fullsize2/BRIP1-FANCJ-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-31883-img0013.jpg)
![Immunocytochemistry: SNM1 Antibody [NBP1-89663] - Staining of human cell line A-431 shows positivity in nucleus and nucleoli.](http://images.novusbio.com/fullsize2/SNM1-Antibody-Immunocytochemistry-NBP1-89663-img0004.jpg)
![Immunohistochemistry-Paraffin: SNM1 Antibody [NBP1-89663] - Staining of human placenta shows strong nuclear positivity in trophoblastic cells.](http://images.novusbio.com/fullsize2/SNM1-Antibody-Immunohistochemistry-Paraffin-NBP1-89663-img0005.jpg)
![Western Blot: XPF Antibody (4E11) [NBP2-01020] Analysis of extracts (35ug) from 9 different cell lines by using anti-XPF monoclonal antibody.](http://images.novusbio.com/fullsize/XPF Antibody (4E11)-Western Blot-NBP2-01020-img0016.jpg)
![Immunocytochemistry/Immunofluorescence: XPF Antibody (4E11) [NBP2-01020] - Staining of COS7 cells transiently transfected by pCMV6-ENTRY XPF.](http://images.novusbio.com/fullsize/XPF Antibody (4E11)-Immunocytochemistry-Immunofluorescence-NBP2-01020-img0015.jpg)
![Western Blot: Frataxin Antibody (1C12) [NBP2-01743] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Frataxin (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-Frataxin.](http://images.novusbio.com/fullsize/Frataxin Antibody (1C12)-Western Blot-NBP2-01743-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: Frataxin Antibody (1C12) [NBP2-01743] Staining of COS7 cells transiently transfected by pCMV6-ENTRY Frataxin.](http://images.novusbio.com/fullsize/Frataxin Antibody (1C12)-Immunocytochemistry-Immunofluorescence-NBP2-01743-img0009.jpg)
![Western Blot: DCLRE1B Antibody (OTI2B7) [NBP2-03563] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY DCLRE1B (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-DCLRE1B.](http://images.novusbio.com/fullsize2/DCLRE1B-Antibody-(OTI2B7)-Western-Blot-NBP2-03563-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: DCLRE1B Antibody (OTI2B7) [NBP2-03563] - Staining of COS7 cells transiently transfected by pCMV6-ENTRY DCLRE1B .](http://images.novusbio.com/fullsize2/DCLRE1B Antibody (OTI2B7)-Immunocytochemistry-Immunofluorescence-NBP2-03563-img0009.jpg)
![Knockout Validated: FUS Antibody [NB100-565] - Western blot shows lysates of HEK293 human embryonic kidney parental cell line and FUS knockout (KO) HEK293 human embryonic kidney cell line. PVDF membrane was probed with 1:1000 of Rabbit Anti-Human FUS Polyclonal Antibody (Catalog # NB100-565) followed by HRP-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog #HAF008). Specific band was detected for FUS at approximately 75 kDa (as indicated) in the parental HEK293 celll line, but is not detectable in the knockout HEK293 cell line. This experiment was conducted under reducing conditions.](http://images.novusbio.com/fullsize2/FUS-Antibody-Knockout-Validated-NB100-565-img0020.jpg)
![Western Blot: FUS Antibody [NB100-565] - FUS activates GSK-3beta in transfected cells and transgenic mice A. Cells were transfected with either control vector (CTRL), HA-FUS, HA-FUSR521C or HA FUSR518K and the samples probed on immunoblots for GSK-3beta phosphorylated on serine 9 (GSK-3beta-S9), total GSK-3beta, FUS (using FUS antibody) and tubulin as a loading control. Phosphorylation of GSK-3beta serine 9 is the principal mechanism for regulating its activity; serine 9 phosphorylation inhibits GSK-3beta activity. Bar chart shows relative levels of GSK-3beta serine 9 phosphorylation following quantification of signals from immunoblots and normalization to total GSK-3beta signals. Data were analysed by one-way ANOVA and Tukey's post hoc test. N = 4, error bars are s.e.m.; *P < 0.05. Image collected and cropped by CiteAb from the following publication (https://onlinelibrary.wiley.com/doi/10.15252/embr.201541726), licensed under a CC-BY licence.](http://images.novusbio.com/fullsize2/FUS Antibody-Western Blot-NB100-565-img0023.jpg)
![Western Blot: FACA/FANCA Antibody [NB100-2564] - Detection of FANC A in transfected COS1 cell lysate.](http://images.novusbio.com/fullsize2/FACA-FANCA-Antibody-Western-Blot-NB100-2564-img0004.jpg)
![Simple Western: PCNA Antibody (PC10) [NB500-106] - Image shows a specific band for PCNA in 0.5 mg/mL of HeLa lysate. This experiment was performed under reducing conditions using the 12-230 kDa separation system.](http://images.novusbio.com/fullsize2/PCNA-Antibody-(PC10)-Simple-Western-NB500-106-img0008.jpg)
![Immunocytochemistry/Immunofluorescence: PCNA Antibody (PC10) [NB500-106] - NIH3T3 cells were fixed and permeabilized for 10 minutes using -20C MeOH. The cells were incubated with anti-PCNA Antibody (PC10) NB500-106 at 1 ug/ml overnight at 4C and detected with an anti-mouse Dylight 488 (Green) at a 1:1000 dilution for 60 minutes. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 100X objective and digitally deconvolved.](http://images.novusbio.com/fullsize2/PCNA-Antibody-(PC10)-Immunocytochemistry-Immunofluorescence-NB500-106-img0015.jpg)
![Western Blot: Fascin Antibody (FSCN1/417) - Azide and BSA Free [NBP2-47801] - HeLa Cell Lysate using Fascin-1 Monoclonal Antibody (FSN1/417)](http://images.novusbio.com/fullsize2/Fascin-Antibody-(FSCN1-417)---Azide-and-BSA-Free-Western-Blot-NBP2-47801-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: Fascin Antibody (FSCN1/417) - Azide and BSA Free [NBP2-47801] - Immunofluorescence Analysis of HeLa cells labeling Fascin with Fascin Antibody (FSCN1/417)-CF640 (Green). The nuclear counterstain is Hoescht (Blue). Membrane is Phalloidin 488 (Red) .](http://images.novusbio.com/fullsize2/Fascin-Antibody-(FSCN1-417)---Azide-and-BSA-Free-Immunocytochemistry-Immunofluorescence-NBP2-47801-img0006.jpg)
![Western Blot: LXR beta/NR1H2 Antibody [NB100-74457] - 25 ug of rat liver (Lane 1), mouse liver (Lane 2) and Hela (Lane 3) cell lysates.](http://images.novusbio.com/fullsize2/LXR beta-NR1H2 Antibody-Western Blot-NB100-74457-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: LXR beta/NR1H2 Antibody [NB100-74457] - Analysis of LXR beta (green) showing positive staining in the nuclear envelope of C2C12 cells (right) compared with a negative control in the absence of primary antibody (left).](http://images.novusbio.com/fullsize2/LXR-beta-NR1H2-Antibody-Immunocytochemistry-Immunofluorescence-NB100-74457-img0003.jpg)
![Western Blot: Rad51 Antibody (14B4) [NB100-148] - eIF3f facilitates hMSH4 stabilization. Western blotting analysis of the levels of HDAC3, hRad51, and VBP1 expression in 293T, 293T/eIF3f, and 293T/eIF3f-hMSH4 cells. 293T/eIF3f-hMSH4 cells treated with 1 or 10 Gy IR were fractionated at 6 hrs post-treatment and the levels of hMSH4 and eIF3f in the nuclear and cytoplasmic fractions were determined by immunoblotting. Alpha-tubulin was used as a marker for the cytoplasmic fraction. Image collected and cropped by CiteAb from the following publication (https://molecular-cancer.biomedcentral.com/articles/10.1186/1476-4598-12-51) licensed under a CC-BY licence.](http://images.novusbio.com/fullsize2/Rad51-Antibody-(14B4)-Western-Blot-NB100-148-img0020.jpg)
![Immunocytochemistry/Immunofluorescence: Rad51 Antibody (14B4) [NB100-148] - HCC1937 (human immortalized breast cancer) cells treated with PARPi for 96 h. Nuclei are stained in blue (DAPI) and RAD51 in red. ICC/IF image submitted by a verified customer review.](http://images.novusbio.com/fullsize2/Rad51-Antibody-(14B4)-Immunocytochemistry-Immunofluorescence-NB100-148-img0021.jpg)
![Western Blot: DNA polymerase theta Antibody (1C11) [H00010721-M09]](http://images.novusbio.com/fullsize2/DNA-polymerase-theta-Antibody-(1C11)-Western-Blot-H00010721-M09-img0002.jpg)
![ELISA: DNA polymerase theta Antibody (1C11) [H00010721-M09] - Detection limit for recombinant GST tagged POLQ is approximately 1ng/ml as a capture antibody.](http://images.novusbio.com/fullsize2/DNA-polymerase-theta-Antibody-(1C11)-ELISA-H00010721-M09-img0001.jpg)
