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Congenital Hypotrichia: Disease Bioinformatics

Research of Congenital Hypotrichia has been linked to Hypotrichosis, Dysplasia, Milium Cyst, Dystrophy, Basal Cell Carcinoma. The study of Congenital Hypotrichia has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Congenital Hypotrichia include Anagen, Pathogenesis, Telogen, Keratinization, Hair Follicle Morphogenesis. These pathways complement our catalog of research reagents for the study of Congenital Hypotrichia including antibodies and ELISA kits against CDH3, P-CADHERIN, CDH15, DSG4, CDH1.

Congenital Hypotrichia 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 Congenital Hypotrichia 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 1081 products for the study of Congenital Hypotrichia that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

AF761
    Simple  Western lane view shows lysates of mouse embryo tissue, loaded at  0.2 mg/mL. A specific band was detected for P‑Cadherin at  approximately 115 kDa (as indicated) using 25 µg/mL of Goat  Anti-Mouse P‑Cadherin Antigen Affinity-purified Polyclonal  Antibody (Catalog # AF761) followed by 1:50 dilution of HRP-conjugated  Anti-Goat IgG Secondary Antibody (Catalog # <a class=P‑Cadherin was detected in immersion fixed frozen sections of mouse embryo (15 dpc) using Goat Anti-Mouse<br>P‑Cadherin Antigen Affinity-purified Polyclonal Antibody (Catalog # AF761) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # <a class=

Goat Polyclonal
Species Mouse
Applications WB, Simple Western, Flow

     1 Review

4 Publications
NBP1-88101
Immunocytochemistry/Immunofluorescence: M-Cadherin/Cadherin-15 Antibody [NBP1-88101] - Staining of human cell line RH-30 shows localization to cytosol & the Golgi apparatus. Antibody staining is shown in green.Immunohistochemistry-Paraffin: M-Cadherin/Cadherin-15 Antibody [NBP1-88101] - Staining of human cerebellum shows weak cytoplasmic positivity in cells in granular layer.

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

AF6589
Western blot shows lysates of human skin tissue. PVDF Membrane was probed with 0.1 µg/mL of Human Desmoglein-4 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF6589) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # <a class=

Sheep Polyclonal
Species Human
Applications WB

1 Publication
AF748
E‑Cadherin was detected in immersion fixed D3 mouse embryonic stem cell line using Goat Anti-Human/Mouse<br>E‑Cadherin Antigen Affinity-purified Polyclonal Antibody (Catalog # AF748) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (red; Catalog # <a class=E‑Cadherin was detected in perfusion fixed frozen sections of mouse skin using Goat Anti-Human/Mouse E‑Cadherin Antigen Affinity-purified Polyclonal Antibody (Catalog # AF748) at 1.7 µg/mL overnight at 4 °C. Tissue was stained using the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (red; Catalog # <a class=

Goat Polyclonal
Species Human, Mouse
Applications WB, Simple Western, Flow

     7 Reviews

34 Publications
3944-ED


Species Human

2 Publications
NBP1-85892
Immunohistochemistry-Paraffin: HAAO Antibody [NBP1-85892] - Staining of human small intestine.Immunohistochemistry-Paraffin: HAAO Antibody [NBP1-85892] - Staining of human liver shows high expression.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

NBP1-33610
Immunohistochemistry: Loricrin Antibody [NBP1-33610] - Prominent differences in the expressions of innate immune and barrier molecules between sebaceous gland poor (SGR) and sebaceous gland rich (SGP) skin regions. Representative images for immunostaining and quantification of epidermal levels of LOR in SGP and SGR skin sections. Images of negative control stainings are shown in the bottom left corner of SGP immunostainings. Size bars=100um. The graphs show the mean +/- SEM of measured protein levels (*p<0.05; **p<0.01; ***p<0.001, as determined by Mann-Whitney U-test). Image collected and cropped by CiteAb from the following publication (frontiersin.org/articles/10.3389/fimmu.2018.00424/full), licensed under a CC-BY licence.Western Blot: Loricrin Antibody [NBP1-33610] - Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with Loricrin antibody [N1], N-term diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, Simple Western, ICC/IF

     3 Reviews

2 Publications
NBP1-48309
Immunocytochemistry: N-Cadherin Antibody (13A9) [NBP1-48309] - Immunostaining of original tumor, low passage, and high passage KCI-MENG1 cells. The original patient-derived tumor (top row) showed moderate and patchy immunoreactivity for epithelial membrane antigen (EMA); strong and diffuse immunostaining for progesterone receptor (PR); and a Ki-67 proliferative index of 2-3%. There was also strong immunostaining for N-cadherin and vimentin. KCI-MENG1-LP cells (middle row) and KCI-MENG1-HP cells (bottom row) maintained expression of EMA, N-cadherin, and vimentin but had significantly reduced PR expression compared to the original tumor. Whereas Ki-67 labeling was found in only a small number of cells in the original tumor and low passage cells, it was positive in virtually all P84 cells. Scale bar 50 um. Image collected and cropped by CiteAb from the following publication (http://www.translational-medicine.com/content/13/1/227), licensed under a CC-BY licence.Western Blot: N-Cadherin Antibody (13A9) [NBP1-48309] - Analysis of N Cadherin expression in HeLa whole cell lysate.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, Simple Western, Flow

     1 Review

31 Publications
NBP2-27372
Western Blot: Cadherin-4/R-Cadherin Antibody [NBP2-27372] - Analysis of R Cadherin in A) human and B) mouse brain lysate using R Cadherin antibody at 3 ug/ml.

Rabbit Polyclonal
Species Human, Mouse, Mammal
Applications WB

3 Publications
NBL1-12400
Western Blot: KRT86 Overexpression Lysate (Adult Normal) [NBL1-12400] Left-Empty vector transfected control cell lysate (HEK293 cell lysate); Right -Over-expression Lysate for KRT86.


Species Human

H00008458-M06
Western Blot: TTF2 Antibody (1E8) [H00008458-M06] - Analysis of TTF2 expression in NIH/3T3 (Cat # L018V1).Immunocytochemistry/Immunofluorescence: TTF2 Antibody (1E8) [H00008458-M06] - Analysis of monoclonal antibody to TTF2 on HeLa cell. Antibody concentration 10 ug/ml

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

H00003889-P01
SDS-Page: Recombinant Human KRTHB3 Protein [H00003889-P01] - 12.5% SDS-PAGE Stained with Coomassie Blue.


Species Human

973-TM


Species Human

     2 Reviews

20 Publications
NB100-214
Western Blot: Blooms Syndrome Protein Blm Antibody [NB100-214] - Samples: Whole cell lysate (15 ug) from HEK293T, K-562, Jurkat, HeLa, and A-549 cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-BLM antibody NB100-214 (lot 4) used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.Western Blot: Blooms Syndrome Protein Blm Antibody [NB100-214] - Samples: Whole cell lysate (50 ug) from TCMK-1 and BIH 3T3 cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-BLM antibody NB100-214 (lot 4) used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 75 seconds.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, IP

7 Publications
NB100-57840
Western Blot: Connexin 26/GJB2 Antibody [NB100-57840] - Staining of Mouse Brain lysate with antibody at 0.01 ug/mL (A), Mouse Heart (B) and Rat Heart (C) lysate with antibody at 0.5 ug/mL (35 ug protein in RIPA buffer). Detected by chemiluminescence.Flow Cytometry: Connexin 26/GJB2 Antibody [NB100-57840] - Flow cytometric analysis of paraformaldehyde fixed HepG2 cells (blue line), permeabilized with 0.5% Triton. Primary incubation 1hr (10 ug/mL) followed by Alexa Fluor 488 secondary antibody (1 ug/mL). IgG control: Unimmunized goat IgG (black line) followed by Alexa Fluor 488 secondary antibody.

Goat Polyclonal
Species Human, Mouse, Rat
Applications WB, Flow, PEP-ELISA

1 Publication

Related Genes

Congenital Hypotrichia has been researched against:

Alternate Names

Congenital Hypotrichia is also known as Congenital Hypotrichosis, Hypotrichosis Congenita.