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Christ-siemens-touraine Syndrome: Disease Bioinformatics

Research of Christ-siemens-touraine Syndrome has been linked to Ectodermal Dysplasia, Dysplasia, Hypohidrosis, Developmental Absence Of Tooth, Hypodontia. The study of Christ-siemens-touraine Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Christ-siemens-touraine Syndrome include Pathogenesis, Odontogenesis, Localization, Secretion, Hair Follicle Development. These pathways complement our catalog of research reagents for the study of Christ-siemens-touraine Syndrome including antibodies and ELISA kits against XLHED, TABBY, ED1, ECTODYSPLASIN A, TA.

Top Research Reagents

We have 1675 products for the study of Christ-siemens-touraine Syndrome that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

NFkB p105/p50 Antibody (2J10D7) - BSA Free
NB100-56583
Western Blot: NFkB p105/p50 Antibody (2J10D7) [NB100-56583] - Analysis of p50 in HeLa lysate in the A) absence and B) presence of immunizing peptide using p50 antibody at 5 ug/ml.Immunohistochemistry-Paraffin: NFkB p105/p50 Antibody (2J10D7) [NB100-56583] - IHC-P of rabbit aorta using NB100-56583. Secondary antibody: anti-mouse histofine ( Nisherei Bioscience Inc. ref: 414131F). Development: DAB (Dako ref: K346811-2) and counterstained with Hematoxylin. Submitted via verified customer review

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

     1 Review

5 Publications
EDARADD Antibody
NBP1-86440
Western Blot: EDARADD Antibody [NBP1-86440] - Analysis in control (vector only transfected HEK293T lysate) and EDARADD over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).Immunohistochemistry-Paraffin: EDARADD Antibody [NBP1-86440] - Staining of human urinary bladder shows strong cytoplasmic positivity in urothelial cells.

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

1 Publication
IKK gamma Inhibitor Peptide Set
NBP2-26504
In vivo assay: IKK gamma Inhibitor Peptide Set [NBP2-26504] - NBD peptide blocks constitutive NF-kB as shown by EMSA. U266 cells were treated with 100 uM of control or NBD peptide for different time periods. Nuclear extracts were isolated and checked for NF-kB-DNA binding activity.In vivo assay: IKK gamma Inhibitor Peptide Set [NBP2-26504] - NBD peptide blocks constitutive NF-kB activation in human multiple myeloma cells. U266 cells were treated with 100 uM of control (A & B) or NBD peptide (C & D) for 12 hr, cytospun, plated on glass slides, air dried for 1 hr at room temperature and fixed with cold acetone. Slides were blocked with 5% normal goat serum for 1 hr and then incubated with rabbit polyclonal anti-human p65 antibody (A & C) followed by Ig-Alexa 594 second step. In control peptide treated cells, p65 translocates to nucleus (A), whereas NBD peptide prevents translocation of p65 into the nucleus (C). B & D: Nuclear staining with DNA binding dye.


Species Human, Mouse, Rat
Applications In vitro, In vivo, B/N

22 Publications
EDAR Antibody [Unconjugated]
AF745

Goat Polyclonal
Species Mouse
Applications WB, Block

7 Publications
HAND2 Antibody [Unconjugated]
AF3876
HAND2 was detected in immersion fixed paraffin-embedded 13 d.p.c. sections of Mouse Embryo using Goat Anti-Human/Mouse HAND2 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF3876) at 3 µg/mL for 1 hour at room temperature followed by incubation with the Anti-Goat IgG VisUCyte™ HRP Polymer Antibody (Catalog # <a class=NoLineLink href=

Goat Polyclonal
Species Human, Mouse
Applications WB, IHC

5 Publications
EDA2R/TNFRSF27/XEDAR Antibody
AF1093

Goat Polyclonal
Species Human
Applications WB, Block

1 Publication
EDA-A1/Ectodysplasin A1
3944-ED


Species Human
Applications Bind

4 Publications
TNF-alpha [Unconjugated]
210-TA
Recombinant Human TNF-alpha (Catalog # 210-TA) has a molecular weight (MW) of 53.1 kDa as analyzed by SEC-MALS, suggesting that this protein is a homotrimer.  MW may differ from predicted MW due to post-translational modifications (PTMs) present (i.e. Glycosylation).Recombinant Human TNF-alpha (Catalog # 210‑TA) induces cytotoxicity in the L-929 mouse fibroblast cell line in the presence of the metabolic inhibitor actinomycin D. The ED<sub>50</sub> for this effect is 25‑100 pg/mL.


Species Human
Applications BA

     3 Reviews

822 Publications
EGF [Unconjugated]
236-EG
Recombinant Human EGF Protein (Catalog # 236-EG) has a molecular weight (MW) of 6.7 kDa as analyzed by SEC-MALS, suggesting that this protein is a monomer.Recombinant Human EGF (Catalog # 236‑EG) stimulates cell proliferation of the Balb/3T3 mouse embryonic fibroblast cell line. The ED<sub>50</sub> for this effect is 20‑100 pg/mL.


Species Human
Applications BA

861 Publications
Connexin 30/GJB6 Antibody (CL4540)
NBP2-61141
Immunocytochemistry/Immunofluorescence: Connexin 30/GJB6 Antibody (CL4540) [NBP2-61141] - Staining of MCF7 cells using the Anti-GJB6 monoclonal antibody, showing no specific staining of cell junctions. MCF7 cells serves as a negative control based on RNA-seq values. Microtubule- and nuclear probes are visualized in red and blue, respectively (where available). Antibody staining is shown in green.Immunocytochemistry/Immunofluorescence: Connexin 30/GJB6 Antibody (CL4540) [NBP2-61141] - Staining of RT-4 cells using the Anti-GJB6 monoclonal antibody, showing specific staining of cell junctions in green. Microtubule- and nuclear probes are visualized in red and blue, respectively (where available). Antibody staining is shown in green.

Mouse Monoclonal
Species Human
Applications ICC/IF, IHC

1 Publication

Related Genes

Christ-siemens-touraine Syndrome has been researched against:

Related Pathways

Christ-siemens-touraine Syndrome has been linked to:

Related Diseases

Christ-siemens-touraine Syndrome has been studied in relation to diseases such as:

Related PTMs

Christ-siemens-touraine Syndrome has been studied in relation to posttranslational modifications (PTMs) including:

Alternate Names

Christ-siemens-touraine Syndrome is also known as Anhidrotic Ectodermal Dysplasia 1, Christ Siemens Touraine Syndrome, Ectodermal Dysplasia 1, Hypohidrotic Ectodermal Dysplasia, Hypohidrotic Ectodermal Dysplasia Syndrome.