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Weill-marchesani Syndrome: Disease Bioinformatics

Weill-Marchesani Syndrome is a rare genetic disorder that causes abnormal features at birth. Weill-Marchesani Syndrome is characterized by a broad head, short stature, hand abnormalities, and eye defects. The defects of the eye vary dramatically from minimal problems to blindness. There is no cure for Weill-Marchesani Syndrome, but eye surgery can be performed to help vision irregularities.

Weill-marchesani 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 Weill-marchesani 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 1253 products for the study of Weill-marchesani Syndrome that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP1-84722
Immunocytochemistry/Immunofluorescence: Fibrillin 1 Antibody [NBP1-84722] - Staining of human cell line U-251 MG shows localization to cytosol. Antibody staining is shown in green.Immunohistochemistry-Paraffin: Fibrillin 1 Antibody [NBP1-84722] - Staining in human cervix, uterine and cerebral cortex tissues. Corresponding FBN1 RNA-seq data are presented for the same tissues.

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

3 Publications
MAB5270

Mouse Monoclonal
Species Human
Applications WB, IP

H00170691-M01
Western Blot: ADAMTS17 Antibody (3B7) [H00170691-M01] - ADAMTS17 monoclonal antibody (M01), clone 3B7 Analysis of ADAMTS17 expression in A-431.Immunohistochemistry-Paraffin: ADAMTS17 Antibody (3B7) [H00170691-M01] - Analysis of monoclonal antibody to ADAMTS17 on formalin-fixed paraffin-embedded human placenta. Antibody concentration 1.2 ug/ml.

Mouse Monoclonal
Species Human, Mouse
Applications WB, ELISA, IHC

2 Publications
NBP1-84185
Western Blot: ADAMTSL4 Antibody [NBP1-84185] - Analysis in human cell line BEWO.Immunohistochemistry-Paraffin: ADAMTSL4 Antibody [NBP1-84185] - Staining of human placenta shows strong cytoplasmic positivity in trophoblastic cells.

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

2 Publications
NBP2-14798
Immunocytochemistry/Immunofluorescence: ADAMTSL2 Antibody [NBP2-14798] - Staining of human cell line A-431 shows localization to vesicles. Antibody staining is shown in green.Immunohistochemistry-Paraffin: ADAMTSL2 Antibody [NBP2-14798] - Staining of human kidney shows moderate cytoplasmic positivity in cells in tubules.

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

NBP2-38530
Western Blot: Ferredoxin Reductase Antibody [NBP2-38530] - Analysis using Anti-FDXR antibody NBP2-38530 (A) shows similar pattern to independent antibody NBP2-38706 (B).Immunocytochemistry/Immunofluorescence: Ferredoxin Reductase Antibody [NBP2-38530] - Staining  of human cell line U-2 OS shows positivity in mitochondria. Antibody staining is shown in green.

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

NBP1-89781
Western Blot: PP14/Glycodelin Antibody [NBP1-89781] - Analysis in human placenta tissue.Immunohistochemistry-Paraffin: PP14/Glycodelin Antibody [NBP1-89781] - Staining of human testis shows no positivity in cells in seminiferous ducts as expected.

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

NBP2-57788
Immunocytochemistry/Immunofluorescence: LTBP3 Antibody [NBP2-57788] - Staining of human cell line U-2 OS shows localization to nucleoplasm. Antibody staining is shown in green.

Rabbit Polyclonal
Species Human
Applications ICC/IF

NBP1-88411
Immunocytochemistry/Immunofluorescence: Latent TGF-beta bp2/LTBP-2 Antibody [NBP1-88411] - Staining of human cell line U-2 OS shows localization to nucleus. Antibody staining is shown in green.Immunohistochemistry-Paraffin: Latent TGF-beta bp2/LTBP-2 Antibody [NBP1-88411] - Staining of human lung shows strong positivity in extracellular matrix.

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

210-TA
1 µg/lane of Recombinant Human TNF-alpha  was resolved by SDS-PAGE with silver staining, under reducing (R) conditions, showing a band at 17 kDa.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

     32 Reviews

647 Publications
DAR00
 Amphiregulin [HRP] Amphiregulin [HRP]


Species Human

     6 Reviews

9 Publications
NBP1-89146
Immunocytochemistry/Immunofluorescence: AKR1B1 Antibody [NBP1-89146] - Staining of human cell line A-431 shows localization to nucleoplasm & cytosol. Antibody staining is shown in green.Immunohistochemistry-Paraffin: AKR1B1 Antibody [NBP1-89146] - Staining of human liver shows no positivity in hepatocytes as expected.

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

NB100-56603
Western Blot: Androgen R/NR3C4 [p Ser213, p Ser210] Antibody (156C135.2) [NB100-56603] - Analysis using Azide Free version of NB100-56603. LNCaP cells (passage number 38) were serum-starved for 2 days. After serum starvation, cells were (A) left untreated, (B) treated with 100 ng/ml IGF-1 for 4h, or (C) incubated with 20 um LY294002 for 30 mi

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, IHC, IHC-P

13 Publications
NBP1-88169
Western Blot: Fibrillin 2 Antibody [NBP1-88169] - Analysis in human cell lines U2OS and A-431. Corresponding RNA-seq data are presented for the same cell lines. Loading control: Anti-PARP1.Immunohistochemistry-Paraffin: Fibrillin 2 Antibody [NBP1-88169] - Staining in human placenta and prostate tissues using anti-FBN2 antibody. Corresponding FBN2 RNA-seq data are presented for the same tissues.

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

2 Publications
NBP3-05061
Western Blot: MID1 Antibody [NBP3-05061] - analysis of extracts of HeLa cells, using MID1 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit. Exposure time: 60s.Immunocytochemistry/Immunofluorescence: MID1 Antibody [NBP3-05061] - Analysis of MCF-7 cells using MID1 antibody. Blue: DAPI for nuclear staining.

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

MAB388

Mouse Monoclonal
Species Human
Applications WB, AP

     2 Reviews

9 Publications
AF5867
Western blot shows lysates of P19 mouse embryonal carcinoma cell line and OVCAR‑3  human ovarian carcinoma cell line. PVDF Membrane was probed with 1 µg/mL of Sheep Anti-Human/Mouse ADAMTS1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5867) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # <A class=NoLineLink href=<P align=left>ADAMTS1 was detected in immersion fixed frozen sections of mouse embryo (13 d.p.c.) using Sheep Anti-Human/Mouse ADAMTS1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5867) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Sheep HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # <A class=NoLineLink href=

Sheep Polyclonal
Species Human, Mouse
Applications WB, IHC, IP

5 Publications
NBP2-14010
Immunohistochemistry-Paraffin: FBN3 Antibody [NBP2-14010] Staining of human kidney shows strong cytoplasmic positivity in cells in tubules.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

NBP2-24916
Western Blot: Catalase Antibody [NBP2-24916] - Analysis in liver lysate of 1) human 2) mouse and 3) rat at 0.1 ug/ml.Immunohistochemistry-Paraffin: Catalase Antibody [NBP2-24916] - Staining of human liver tissue using an isotype control (top) and this antibody (bottom) at 5 ug/ml.

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

     1 Review

6 Publications

Related Genes

Weill-marchesani Syndrome has been researched against:

Related PTMs

Weill-marchesani Syndrome has been studied in relation to posttranslational modifications (PTMs) including:

Alternate Names

Weill-marchesani Syndrome is also known as weill-marchesani syndrome, spherophakia-brachymorphia syndrome, weill-marchesani syndrome, autosomal recessive, mesodermal dysmorphodystrophy, congenital, congenital mesodermal dysmorphodystrophy, mesodermal dysmorphodystrophy congenital, spherophakia brachymorphia syndrome, congenital mesodermal dystrophy, neonatal hemochromatosis, marchesani syndrome, wm syndrome.