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Fazio-londe Syndrome: Disease Bioinformatics

Research of Fazio-londe Syndrome has been linked to Bulbar Palsy, Progressive, Bulbar Palsy, Progressive, With Sensorineural Deaf, Complete Hearing Loss, Sensorineural Hearing Loss (disorder), Motor Neuron Disease. The study of Fazio-londe Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Fazio-londe Syndrome including antibodies and ELISA kits against C20ORF54, SLC52A1, SLC52A2, SLC52A3, MADD.

Fazio-londe 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 Fazio-londe 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 77 products for the study of Fazio-londe Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

19540002
Immunohistochemistry: GPR172B Antibody [19540002] - Lymphomas and malignant gliomas were moderately stained in cytoplasm whilst their normal counterparts were negative.  Image was provided courtesy of the Swedish Human Proteome Resource (HPR) Center.Immunohistochemistry: GPR172B Antibody [19540002] - IHC using anti GPR172B SEQer antibody

Rabbit Polyclonal
Species Human
Applications ELISA, IHC, IHC-P

2 Publications
NBP2-49382
Immunohistochemistry: GPR172A Antibody [NBP2-49382] - Staining of human small intestine shows moderate cytoplasmic and membranous positivity in glandular cells.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

NBP2-14683
Immunohistochemistry-Paraffin: SLC52A3 Antibody [NBP2-14683] Staining of human testis shows strong cytoplasmic positivity in subset of cells in seminiferus ducts.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

NBP1-77033
Western Blot: MADD Antibody [NBP1-77033] - Whole cell lysates from the indicated cell lines with MADD antibody at 1:250 dilution.Immunocytochemistry/Immunofluorescence: MADD Antibody [NBP1-77033] - Immunofluorescence of MADD in Hela cells with MADD antibody at 20 ug/mL.

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

NBP1-83950
Western Blot: ETFDH Antibody [NBP1-83950] - Lane 1: Marker  [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10.  Lane 2: Human cell line RT-4.  Lane 3: Human cell line U-251MG sp.  Lane 4: Human plasma (IgG/HSA depleted).  Lane 5: Human liver tissueImmunohistochemistry-Paraffin: ETFDH Antibody [NBP1-83950] - Staining in human duodenum and pancreas tissues using anti-ETFDH antibody. Corresponding ETFDH RNA-seq data are presented for the same tissues.

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

NBP1-89545
Western Blot: ETFB Antibody [NBP1-89545] - Analysis in mouse cell line NIH-3T3 and rat cell line NBT-II.Immunocytochemistry/Immunofluorescence: ETFB Antibody [NBP1-89545] - Immunofluorescent staining of human cell line U-251 MG shows localization to mitochondria & vesicles.

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

NBP2-16382
Western Blot: ETFA Antibody [NBP2-16382] - Wild-type (WT) and ETFA knockout (KO) 293T cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with ETFA antibody diluted at 1:1000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.Immunocytochemistry/Immunofluorescence: ETFA Antibody [NBP2-16382] - Confocal immunofluorescence analysis of methanol-fixed HeLa, using ETFA antibody (Green) at 1:500 dilution. Alpha-tubulin filaments are labeled with Alpha-tubulin antibody (Red) at 1:2000.

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


Related Genes

Fazio-londe Syndrome has been researched against:

Alternate Names

Fazio-londe Syndrome is also known as fazio londe syndrome, fazio-londe disease, bulbar hereditary motor neuronopathy (hmn) type ii, progressive bulbar paralysis of childhood, progressive bulbar palsy of childhood, childhood progressive bulbar palsy, bulbar palsy, progressive, fazio-londe syndrome, bulbar hmn ii.