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Ochoa Syndrome: Disease Bioinformatics

Research of Ochoa Syndrome has been linked to Urologic Diseases, Neurogenic Urinary Bladder, Urinary Tract Infection, Kidney Failure, Gastroesophageal Reflux Disease. The study of Ochoa Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Ochoa Syndrome include Micturition, Amelogenesis, Localization. These pathways complement our catalog of research reagents for the study of Ochoa Syndrome including antibodies and ELISA kits against AMBP, CBS, GOT1, MB, PVR.

Ochoa Syndrome 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 Ochoa Syndrome below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 288 products for the study of Ochoa Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP1-31457
Western Blot: HPSE2 Antibody [NBP1-31457] - Sample(30 ug whole cell lysate)A:293T B:H1299 C:HeLa S3 7.5% SDS PAGE, antibody diluted at 1:1000.Immunohistochemistry-Paraffin: HPSE2 Antibody [NBP1-31457] - Paraffin-embedded Uterus, using antibody 10 ug/ml.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, IHC, IHC-P

NBP1-89280
Immunocytochemistry/Immunofluorescence: CNNM4 Antibody [NBP1-89280] - Staining of human cell line U-2 OS shows positivity in cytoskeleton (actin filaments).Immunohistochemistry-Paraffin: CNNM4 Antibody [NBP1-89280] - Staining of human appendix shows cytoplasmic and membranous positivity in glandular cells.

Rabbit Polyclonal
Species Human
Applications ICC/IF, IHC, IHC-P

1 Publication
NBP1-89281
Immunohistochemistry-Paraffin: CNNM1 Antibody [NBP1-89281] - Staining of human testis shows moderate cytoplasmic positivity in cells in seminiferus ducts and strong positivity in Leydig cells.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, IHC

NBP1-77320
Western Blot: Lgi1 Antibody [NBP1-77320] - HeLa cell lysate with LGI1 antibody at 2 ug/ml.Immunohistochemistry-Paraffin: Lgi1 Antibody [NBP1-77320] - Human brain tissue using LGI1 antibody at 2.5 ug/ml.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, ELISA, IHC

NBP1-48002
Western Blot: SSB Antibody (2C8) [NBP1-48002] Analysis of extracts (35ug) from 9 different cell lines by using anti-SSB monoclonal antibody.Immunocytochemistry/Immunofluorescence: SSB Antibody (2C8) [NBP1-48002] - Staining of COS7 cells transiently transfected by pCMV6-ENTRY SSB.

Mouse Monoclonal
Species Human, Canine, Primate
Applications WB, ICC/IF, IHC

NBP2-38088
Immunohistochemistry: golgi transport 1 homolog B Antibody [NBP2-38088] - Staining of human kidney shows strong granular cytoplasmic positivity in cells in tubules.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

NB110-59906
Western Blot: Capicua Antibody [NB110-59906] - WB detection of Human Capicua /CIC in whole cell lysates of HeLa (5, 15 and 50 ug )  and 293T (T, 50 ug) cells using affinity purified rabbit Capicua antibody NB110-59906 used at 1 ug/ml concentration.Immunocytochemistry/Immunofluorescence: Capicua Antibody [NB110-59906] - Capicua antibody was tested in Neuro 2A cells with DyLight 488 (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and Dylight 550 (red).

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB, ICC/IF, IP

NBP2-57086
Western Blot: CNNM2 Antibody [NBP2-57086] - Western blot analysis in human cell line RT-4.Immunocytochemistry/Immunofluorescence: CNNM2 Antibody [NBP2-57086] - Staining of human cell line HEK 293 shows localization to vesicles.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF

NBP1-54778
Western Blot: Aspartate Aminotransferase Antibody [NBP1-54778] - Titration: 1.0ug/ml, Positive Control: NCI-H226 cell lysate.Western Blot: Aspartate Aminotransferase Antibody [NBP1-54778] - Human Fetal Liver.

Rabbit Polyclonal
Species Human
Applications WB

4 Publications
H00000259-D01P
Western Blot: alpha 1-Microglobulin Antibody [H00000259-D01P] - Analysis of AMBP expression in mouse testis.Western Blot: alpha 1-Microglobulin Antibody [H00000259-D01P] - Analysis of AMBP expression in PC-12.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB

NB110-89456
Western Blot: Myoglobin Antibody (5A2G8) [NB110-89456] - Analysis using Myoglobin mouse mAb against truncated Myoglobin recombinant protein(AA: 2-154).Immunohistochemistry-Paraffin: Myoglobin Antibody (5A2G8) [NB110-89456] - Analysis of paraffin-embedded human skeletal muscle tissue showing cytoplasmic localization using anti-Myoglobin antibody with DAB staining.

Mouse Monoclonal
Species Human
Applications WB, ELISA, IHC

H00000875-M01
Western Blot: CBS Antibody (3E1) [H00000875-M01] - CBS monoclonal antibody (M01), clone 3E1. Analysis of CBS expression in MCF-7.Immunohistochemistry-Paraffin: CBS Antibody (3E1) [H00000875-M01] - Analysis of monoclonal antibody to CBS on formalin-fixed paraffin-embedded human hepatocellular carcinoma. Antibody concentration 3 ug/ml.

Mouse Monoclonal
Species Human, Rat
Applications WB, ELISA, ICC/IF

     1 Review

44 Publications
MAB25301
CD155/PVR was detected in immersion fixed human peripheral blood mononuclear cells (PBMCs) using Mouse Anti-Human CD155/PVR Monoclonal Antibody (Catalog # MAB25301) at 15 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog # <A class=NoLineLink href=    U937  human histiocytic lymphoma cell line was stained with Mouse Anti-Human  CD155/PVR Monoclonal Antibody (Catalog # MAB25301, filled histogram) or  isotype control antibody (Catalog # <a class=

Mouse Monoclonal
Species Human
Applications WB, Flow, CyTOF-ready

     1 Review

5 Publications

Related Genes

Ochoa Syndrome has been researched against:

Related Pathways

Ochoa Syndrome has been linked to:

Alternate Names

Ochoa Syndrome is also known as ochoa syndrome, partial facial palsy with urinary abnormalities, urofacial syndrome, ufs, inverted smile-neurogenic bladder, hydronephrosis-inverted smile, chromosome inversion, hydronephrosis, partialism.