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Marie Unna Hereditary Hypotrichosis: Disease Bioinformatics

Research of Marie Unna Hereditary Hypotrichosis has been linked to Hypotrichosis, Pili Torti, Congenital Hypotrichia, Cicatrix, Hair Diseases. The study of Marie Unna Hereditary Hypotrichosis has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Marie Unna Hereditary Hypotrichosis include Hair Follicle Morphogenesis, Translation, Hair Follicle Development, Anagen, Pathogenesis. These pathways complement our catalog of research reagents for the study of Marie Unna Hereditary Hypotrichosis including antibodies and ELISA kits against HR, HAIRLESS, DLC1, EPB49, HP.

Marie Unna Hereditary Hypotrichosis 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 Marie Unna Hereditary Hypotrichosis 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 302 products for the study of Marie Unna Hereditary Hypotrichosis that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

AF5708
Western blot shows lysates of HEK293 human embryonic kidney cell line. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human Hairless Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5708) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # <A class=NoLineLink href=Hairless was detected in immersion fixed human NHEK epidermal keratinocytes using 10 µg/mL Goat Anti-Human Hairless Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5708) for 3 hours at room temperature. Cells were stained with the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (red; Catalog # <a class=

Goat Polyclonal
Species Human
Applications WB, ICC

1 Publication
NBP1-88824
Western Blot: DLC1 Antibody [NBP1-88824] - Lane 1: NIH-3T3 cell lysate (Mouse embryonic fibroblast cells) Lane 2: NBT-II cell lysate (Rat Wistar bladder tumour cells)Immunocytochemistry/Immunofluorescence: DLC1 Antibody [NBP1-88824] - Immunofluorescent staining of human cell line U-251 MG shows localization to nucleoplasm & vesicles.

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

1 Publication
NBP1-85007
Immunohistochemistry-Paraffin: Dematin Antibody [NBP1-85007] - Staining of human tonsil shows strong cytoplasmic positivity in subsets of cells.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

1 Publication
NBP2-66881
Western Blot: Haptoglobin Antibody (JM10-79) [NBP2-66881] - Analysis of Haptoglobin on different cells lysates using anti-Haptoglobin antibody at 1/500 dilution. Positive control: Lane 1: Hela Lane 2: HepG2Immunocytochemistry/Immunofluorescence: Haptoglobin Antibody (JM10-79) [NBP2-66881] - Staining Haptoglobin in HepG2 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.

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

NB100-56126
Western Blot: Caspase-14 Antibody [NB100-56126] -  Analysis of Caspase-14. Tissue lysates (50 ug/lane) and recombinant human Caspase-14 were (Hu C14, 15 ng) were western blotted with Caspase-14 antibody at 1:2000. The antibody detected both the proform of caspase-14, and the large and small subunits of active/cleaved caspase-14.Immunohistochemistry: Caspase-14 Antibody [NB100-56126] - Tissue sections of mouse skin at E17 stained using this antibody at 1:500.

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

5 Publications
NBP2-17040
Western Blot: Cytokeratin 71 Antibody [NBP2-17040] - Cytokeratin 71 Sample (30 ug of whole cell lysate) A: HepG2 7. 5% SDS PAGE gel, diluted at 1:5000.Immunocytochemistry/Immunofluorescence: Cytokeratin 71 Antibody [NBP2-17040] - HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: KRT71 protein stained by KRT71 antibody [N3C3] diluted at 1:500. Blue: Hoechst 33342 staining. Scale bar = 10 um.

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

2 Publications
NBP2-13966
Immunocytochemistry/Immunofluorescence: EPS8L3 Antibody [NBP2-13966] - Immunofluorescent staining of human cell line U-2 OS shows localization to vesicles.Immunohistochemistry-Paraffin: EPS8L3 Antibody [NBP2-13966] - Staining of human lung shows strong membranous positivity in alveolar and endothelial cells.

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

MAB134
WIF‑1 was detected in immersion fixed paraffin-embedded sections of human breast using 8 µg/mL Mouse Anti-Human WIF‑1 Monoclonal Antibody (Catalog # MAB134) overnight at 4 °C. Tissue was stained with the Anti-Mouse HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # <A class=

Mouse Monoclonal
Species Human
Applications WB, IHC

     1 Review

3 Publications
5396-SF


Species Human

13 Publications
MAB97203
    Myoglobin  was detected in immersion fixed paraffin-embedded sections of human heart  using Rabbit Anti-Human Myoglobin Monoclonal Antibody (Catalog # MAB97203) at  3 µg/mL for 1 hour at room temperature followed by  incubation with the Anti-Rabbit IgG VisUCyte™ HRP Polymer Antibody  (Catalog # <a class=    Western  blot shows lysates of human heart tissue, mouse heart tissue, rat heart  tissue, and human liver tissue. PVDF membrane was probed with  0.5 µg/mL of Rabbit Anti-Human Myoglobin Monoclonal Antibody  (Catalog # MAB97203) followed by HRP-conjugated Anti-Rabbit IgG Secondary  Antibody (Catalog # <a class=

Rabbit Monoclonal
Species Human, Mouse, Rat
Applications WB, Simple Western, ELISA

1169-FR/CF


Species Mouse

8 Publications

Related Genes

Marie Unna Hereditary Hypotrichosis has been researched against:

Related Pathways

Marie Unna Hereditary Hypotrichosis has been linked to:

Alternate Names

Marie Unna Hereditary Hypotrichosis is also known as Hypotrichosis, Marie Unna Type, Marie Unna Congenital Hypotrichosis.