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Metabolic Brain Diseases, Inherited: Disease Bioinformatics

Inherited metabolic brain diseases arise from disturbances in body chemistry due to an alteration in the metabolic cycle. A disturbance in the brain’s chemical environment in the form of a deficiency or the buildup of metabolites leading to the spread of toxins can lead to a metabolic disorder, which can be expressed in many forms such as impaired brain development, cerebral palsy and seizures. Inherited metabolic brain diseases are passed on genetically, typically in an autosomal recessive manner. The majority of metabolic brain diseases occur in infants and children, but the possibility of a late onset also exists. Treatment for many metabolic brain diseases is still being researched, but many doctors will attempt to restore the chemical balance of the brain in order to reverse the effects of the symptoms.

Metabolic Brain Diseases, Inherited 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 Metabolic Brain Diseases, Inherited below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 421 products for the study of Metabolic Brain Diseases, Inherited that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Western Blot: MiTF Antibody (21D1418) [NB100-56561] - Western blot analysis of HeLa lysate (35ug per lane, RIPA buffer) using MiTF antibody (NB100-56561) at 0.1ug/ml. Band detected at ~60kDa. (Expected MW of 58.2kDa according to NP_937802.1).Western Blot: MiTF Antibody (21D1418) [NB100-56561] - Analysis of A375 lysate using MITF antibody at 4 ug/ml.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB

1 Publication
Western Blot: CRIPTO Antibody [NB100-1598] - Analysis of Cripto in Dicer knockout mouse embryonic stem cell lysate.Immunocytochemistry/Immunofluorescence: CRIPTO Antibody [NB100-1598] - CRIPTO  antibody was tested in HeLa cells with Dylight 488 (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and Dylight 550 (red).

Rabbit Polyclonal
Species Human, Mouse
Applications WB, Flow, ICC/IF

1 Publication
Western Blot: Arginine decarboxylase Antibody [NBP1-70403] - Titration: 0.2-1 ug/ml, Positive Control: COLO205 cell lysate.Western Blot: Arginine decarboxylase Antibody [NBP1-70403] - Sample Type: Human and Rat Cerebral CortexPrimary Dilution: 1:3000.

Rabbit Polyclonal
Species Human
Applications WB

Western Blot: DHRS4 Antibody [NBP1-83790] - Lane 1: Marker [kDa] 230, 130, 95, 72, 56, 36, 28, 17, 11<br/>Lane 2: Human cell line RT-4<br/>Lane 3: Human cell line U-251MG spImmunocytochemistry/Immunofluorescence: DHRS4 Antibody [NBP1-83790] - Staining of human cell line A-431 shows positivity in nuclear membrane & vesicles.

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

CD55/DAF was detected in immersion fixed paraffin-embedded sections of human colon cancer tissue using 15 µg/mL Goat Anti-Human CD55/DAF Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2009) overnight at 4 °C. Tissue was stained with the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # <A class=NoLineLink href=

Goat Polyclonal
Species Human
Applications WB, IHC

2 Publications
Western Blot: Calretinin Antibody [NBP1-88221] - Lane 1: Marker [kDa] 250, 130, 100, 70, 55, 35, 25, 15, 10 Lane 2: Mouse Cerebellum tissueImmunocytochemistry/Immunofluorescence: Calretinin Antibody [NBP1-88221] - Staining of mouse substantia nigra shows neuronal cell bodies and processes in pars compacta.

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

1 Publication

Related Genes

Metabolic Brain Diseases, Inherited has been researched against:

Related Pathways

Related PTMs

Alternate Names

Metabolic Brain Diseases, Inherited is also known as Inherited Metabolic Brain Diseases.