Goldenhar Syndrome With Ipsilateral Radial Defect: Disease Bioinformatics
Research of Goldenhar Syndrome With Ipsilateral Radial Defect has been linked to Mandibulofacial Dysostosis, Facial Asymmetry, Dysplasia, Dermoid Cyst, Fetal Growth Retardation. The study of Goldenhar Syndrome With Ipsilateral Radial Defect has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Goldenhar Syndrome With Ipsilateral Radial Defect include Pathogenesis, Segmentation, Transposition, Cell Migration, Fertilization. These pathways complement our catalog of research reagents for the study of Goldenhar Syndrome With Ipsilateral Radial Defect including antibodies and ELISA kits against LACRIMAL, STRABISMUS, APC, ARHGAP4, C2.
Top Research Reagents
We have 1195 products for the study of Goldenhar Syndrome With Ipsilateral Radial Defect that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Goldenhar Syndrome With Ipsilateral Radial Defect is also known as Facio-auriculo-vertebral Spectrum, Facioauriculovertebral Sequence, First And Second Branchial Arch Syndrome, First Arch Syndrome, Goldenhar Syndrome.
![Western Blot: Ceruloplasmin Antibody (6C3K9) [NBP3-15868] - Analysis of extracts of various cell lines, using Ceruloplasmin antibody (NBP3-15868) at 1:5000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 1s.](https://images.novusbio.com/fullsize/Ceruloplasmin-Antibody-6C3K9-Western-Blot-NBP3-15868-img0006.jpg)
![Immunohistochemistry: Ceruloplasmin Antibody (6C3K9) [NBP3-15868] - Immunofluorescence analysis of mouse liver using Ceruloplasmin Rabbit mAb (NBP3-15868) at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/Ceruloplasmin-Antibody-6C3K9-Immunohistochemistry-NBP3-15868-img0005.jpg)
![Western Blot: MST4 Antibody [NBP3-35679] - Western blot analysis of lysates from rat thymus, using MST4 Rabbit pAb at 1:1000 dilution.<br/>Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.<br/>Lysates/proteins: 25ug per lane.<br/>Blocking buffer: 3% nonfat dry milk in TBST.<br/>Detection: ECL Basic Kit.<br/>Exposure time: 3s.](https://images.novusbio.com/fullsize/nbp3-35679_rabbit-mst4-pab-9122024158124.jpg)
![Immunohistochemistry: MST4 Antibody [NBP3-35679] - Immunohistochemistry analysis of paraffin-embedded Human thyroid cancer using MST4 Rabbit pAb at dilution of 1:100 (40x lens). Microwave antigen retrieval performed with 0.01M PBS Buffer (pH 7.2) prior to IHC staining.](https://images.novusbio.com/fullsize/nbp3-35679_rabbit-mst4-pab-9122024141811.jpg)
![Immunocytochemistry/ Immunofluorescence: MRPL28 Antibody [NBP3-38209] - Immunofluorescence analysis of U2OS cells using MRPL28 Rabbit pAb. Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/nbp3-38209_rabbit-mrpl28-pab-101220241143345.jpg)
![Immunoprecipitation: MRPL28 Antibody [NBP3-38209] - Immunoprecipitation analysis of 200 ug extracts of 293T cells using MRPL28 antibody. Western blot was performed from the immunoprecipitate using MRPL28 antibody at a dilution of 1:1000.](https://images.novusbio.com/fullsize/nbp3-38209_rabbit-mrpl28-pab-1012202411421088.jpg)
![Western Blot: p23/PTGES3 Antibody (JJ3) [NB300-576] - Analysis of 25 ug of Hela (Lane 1), HepG2 (Lane 2), and mouse spleen cell lysates (Lane 3) and a molecular weight protein ladder.](https://images.novusbio.com/fullsize/p23-PTGES3-Antibody-JJ3-Western-Blot-NB300-576-img0010.jpg)
![Immunocytochemistry/Immunofluorescence: p23/PTGES3 Antibody (JJ3) [NB300-576] - p23 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with or an antibody recognizing p23 at a dilution of 1:500 over night at 4C, washed with PBS and incubated with a DyLight-488 conjugated.](https://images.novusbio.com/fullsize/p23-PTGES3-Antibody-JJ3-Immunocytochemistry-Immunofluorescence-NB300-576-img0006.jpg)
![Western Blot: SUB1 Antibody [NBP1-82454] - Analysis in human cell line RPMI-8226.](https://images.novusbio.com/fullsize/SUB1-Antibody-Western-Blot-NBP1-82454-img0009.jpg)
![Immunocytochemistry/Immunofluorescence: SUB1 Antibody [NBP1-82454] - Staining of human cell line U-2 OS shows localization to nucleus & nucleoli. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/SUB1-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-82454-img0011.jpg)
![Western Blot: Treacher Collins syndrome protein Antibody [NBP1-86908] - Analysis in human cell line CACO-2.](https://images.novusbio.com/fullsize/Treacher-Collins-syndrome-protein-Antibody-Western-Blot-NBP1-86908-img0017.jpg)
![Immunocytochemistry/Immunofluorescence: Treacher Collins syndrome protein Antibody [NBP1-86908] - Staining of human cell line U-2 OS shows localization to nucleoli fibrillar center. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/Treacher-Collins-syndrome-protein-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-86908-img0007.jpg)
![Immunohistochemistry-Paraffin: ARHGAP4 Antibody [NBP1-88527] - Staining in human spleen and cerebral cortex tissues using anti-ARHGAP4 antibody. Corresponding ARHGAP4 RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/ARHGAP4-Antibody-Immunohistochemistry-Paraffin-NBP1-88527-img0012.jpg)
![Immunohistochemistry-Paraffin: ARHGAP4 Antibody [NBP1-88527] - Staining of human colon, liver, lymph node and testis using Anti-ARHGAP4 antibody NBP1-88527 (A) shows similar protein distribution across tissues to independent antibody NBP1-88528 (B).](https://images.novusbio.com/fullsize/ARHGAP4-Antibody-Immunohistochemistry-Paraffin-NBP1-88527-img0013.jpg)
![Western Blot: SS18L1 Antibody [NBP2-20486] - Sample (50 ug of whole cell lysate) A: Mouse Brain, 10% SDS PAGE gel, diluted at 1:1000.](https://images.novusbio.com/fullsize/SS18L1-Antibody-Western-Blot-NBP2-20486-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: SS18L1 Antibody [NBP2-20486] - Immunofluorescence analysis of paraformaldehyde-fixed A431, using antibody at 1:500 dilution.](https://images.novusbio.com/fullsize/SS18L1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-20486-img0004.jpg)
![Western Blot: hnRNP C1 + C2 Antibody (CL2593) [NBP2-36776] - Analysis in U-251MG cells transfected with control siRNA, target specific siRNA probe #1 and #2, using Anti-HNRNPC antibody. Remaining relative intensity is presented. Loading control: Anti-PPIB.](https://images.novusbio.com/fullsize/hnRNP-C1-+-C2-Antibody-CL2593-Western-Blot-NBP2-36776-img0015.jpg)
![Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (CL2593) [NBP2-36776] - Staining in U2OS cell line with Anti-HNRNPC monoclonal antibody, showing distinct nuclear (without nucleoli) staining in green. Microtubule- and nuclear probes are visualized in red and blue respectively (where available). Antibody staining is shown in green.](https://images.novusbio.com/fullsize/hnRNP-C1-+-C2-Antibody-CL2593-Immunocytochemistry-Immunofluorescence-NBP2-36776-img0014.jpg)
![Western Blot: p15INK4b/CDKN2B Antibody (OTI3B6) [NBP2-45603] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY CDKN2B.](https://images.novusbio.com/fullsize/p15INK4b-CDKN2B-Antibody-OTI3B6-Western-Blot-NBP2-45603-img0005.jpg)
![Immunohistochemistry: p15INK4b/CDKN2B Antibody (OTI3B6) [NBP2-45603] - Analysis of Adenocarcinoma of Human endometrium tissue.](https://images.novusbio.com/fullsize/p15INK4b-CDKN2B-Antibody-OTI3B6-Immunohistochemistry-NBP2-45603-img0004.jpg)
![Western Blot: NXT1 Antibody (4F11) [H00029107-M08] - Analysis of NXT1 expression in transfected 293T cell line by NXT1 monoclonal antibody (M08), clone 4F11. Lane 1: NXT1 transfected lysatE (15.51 KDa). Lane 2: Non-transfected lysate.](https://images.novusbio.com/fullsize/NXT1-Antibody-4F11-Western-Blot-H00029107-M08-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: NXT1 Antibody (4F11) [H00029107-M08] - Analysis of monoclonal antibody to NXT1 on HeLa cell. Antibody concentration 10 ug/ml](https://images.novusbio.com/fullsize/NXT1-Antibody-4F11-Immunocytochemistry-Immunofluorescence-H00029107-M08-img0004.jpg)
![Western Blot: Glutamine Synthetase Antibody [NB110-41404] - Analysis of glutamine synthase. 40ug of lysates from mouse (Lanes M), rat (Lane R), pig (Lane P), bovine (Lane B), or human (Lane Hu) retina were probed. A 42 kDa band was identified in lysates from retinas of all species.](https://images.novusbio.com/fullsize/Glutamine-Synthetase-Antibody-Western-Blot-NB110-41404-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: Glutamine Synthetase Antibody [NB110-41404] - Immunofluorescence using NB110-41404. Submitted via verified customer review.](https://images.novusbio.com/fullsize/Glutamine-Synthetase-Antibody-Immunocytochemistry-Immunofluorescence-NB110-41404-img0006.jpg)
![Western Blot: APC Antibody [NB100-91662] - Lane1:Hela cell lysate. Lane2:HEK293T cell lysate. Lane3:Rat testis tissue lysate.](https://images.novusbio.com/fullsize/APC-Antibody-Western-Blot-NB100-91662-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: APC Antibody [NB100-91662] - HeLa cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X PBS + 0.05% Triton-X100. The cells were incubated with anti-APC Antibody at 2 ug/ml overnight at 4C and detected with an anti-rabbit Dylight 488 (Green) at a 1:500 dilution. Nuclei were counterstained with DAPI (Blue). Cells were imaged using a 40X objective.](https://images.novusbio.com/fullsize/APC-Antibody-Immunocytochemistry-Immunofluorescence-NB100-91662-img0006.jpg)
![Western Blot: PFDN4 Antibody [NBP2-93935] - Analysis of extracts of various cell lines, using PFDN4 at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit . Exposure time: 90s.](https://images.novusbio.com/fullsize/PFDN4-Antibody-Western-Blot-NBP2-93935-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: PFDN4 Antibody [NBP2-93935] - Analysis of C6 cells using PFDN4 at dilution of 1:100. Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/PFDN4-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-93935-img0007.jpg)
![Immunohistochemistry: Tmp21/p23 Antibody [NB110-57586] - TMP21 Antibody [NB110-57586] - Detection of TMP21 in central neurons.](https://images.novusbio.com/fullsize/TMP21-Antibody-Immunohistochemistry-NB110-57586-img0005.jpg)
![Western Blot: Tmp21/p23 Antibody [NB110-57586] - Western blot shows lysates of HEK293T human embryonic kidney parental cell line and TMP21/TMED10 knockout (KO) HEK293T cell line. PVDF membrane was probed with 2.0 ug/ml of Rabbit Anti-Human TMP21/TMED10 Polyclonal Antibody (Catalog # NB110-57586) followed by HRP-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog #HAF008). Specific band was detected for TMP21/TMED10 at approximately 25 kDa (as indicated) in the parental HEK293T cell line, but is not detectable in the knockout HEK293T cell line. This experiment was conducted under reducing conditions.](https://images.novusbio.com/fullsize/Tmp21-p23-Antibody-Knockdown-Validated-NB110-57586-img0006.jpg)
