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Meckel-gruber Syndrome: Disease Bioinformatics

Research of Meckel-gruber Syndrome has been linked to Congenital Cerebral Hernia, Polycystic Kidney Diseases, Polydactyly, Dysplasia, Cystic Kidney Diseases. The study of Meckel-gruber Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Meckel-gruber Syndrome include Localization, Pathogenesis, Transport, Intraflagellar Transport, Neural Tube Closure. These pathways complement our catalog of research reagents for the study of Meckel-gruber Syndrome including antibodies and ELISA kits against TMEM67, MKS1, MKKS, CEP290, RPGRIP1L.

Meckel-gruber 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 Meckel-gruber 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 625 products for the study of Meckel-gruber Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

NBP1-06590
Western Blot: Meckelin Antibody [NBP1-06590] - Immunodetection of Meckelin (120kDa) in whole cell extracts of HEK293 cells.Immunohistochemistry-Paraffin: Meckelin Antibody [NBP1-06590] - Staining of kidney tissue section with Meckelin Antibody (NBP1-06590).

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

1 Publication
NBP1-88691
Western Blot: MKS1 Antibody [NBP1-88691] - Analysis in human cell line HEK 293.Immunohistochemistry-Paraffin: MKS1 Antibody [NBP1-88691] - Staining of human kidney.

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

1 Publication
NBP1-92123
Western Blot: MKKS Antibody [NBP1-92123] - Lane 1: Marker  [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10.  Lane 2: Human cell line RT-4.  Lane 3: Human cell line U-251MG spImmunocytochemistry/Immunofluorescence: MKKS Antibody [NBP1-92123] - Immunofluorescent staining of human cell line U-2 OS shows localization to centrosome.

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

NB100-86991
Western Blot: CEP290 Antibody [NB100-86991] - Detection of human CEP290 by western blot and immunoprecipitation. Samples: Whole cell lysate from HeLa (5, 15 and 50 ug for WB; 1 mg for IP, 20% of IP loaded) and HEK293T (T; 50 ug) cells. Antibodies: Affinity purified rabbit anti-CEP290 antibody NB100-86991 used for WB at 0.1 ug/ml (A) and 1 ug/ml (B) and used for IP at 3 ug/mg lysate. Detection: Chemiluminescence with exposure times of 30 seconds (A) and 10 second (B).Immunocytochemistry/Immunofluorescence: CEP290 Antibody [NB100-86991] - NBF-fixed asynchronous HeLa cells. Antibody used at a dilution of 1:500.

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

9 Publications
NBP1-84403
Immunohistochemistry-Paraffin: RPGRIP1L Antibody [NBP1-84403] - Staining of human bronchus shows strong cytoplasmic positivity in respiratory epithelial cells.

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

2 Publications
MAB1368
    HepG2  human hepatocellular carcinoma cell line was stained with Mouse  Anti-Human/Mouse  alpha ‑Fetoprotein/AFP Monoclonal Antibody (Catalog #  MAB1368, filled histogram) or isotype control antibody (Catalog #  <a class=    Western  blot shows lysates of HepG2 human hepatocellular carcinoma cell line. PVDF  membrane was probed with 0.5 µg/mL of Mouse Anti-Human/Mouse<br> alpha ‑Fetoprotein/AFP Monoclonal Antibody (Catalog # MAB1368) followed  by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # <a class=

Mouse Monoclonal
Species Human, Mouse
Applications WB, Simple Western, CyTOF-ready

     6 Reviews

26 Publications
NBP1-59110
Western Blot: Nephronophthisis Antibody [NBP1-59110] - Human Heart lysate, concentration 0.2-1 ug/ml.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB

NBP1-93673
Immunohistochemistry-Paraffin: CC2D2A Antibody [NBP1-93673] - Staining of human placenta shows strong nuclear and cytoplasmic positivity in trophoblastic cells.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

1 Publication
NBP2-39059
Immunohistochemistry: NPHP4 Antibody [NBP2-39059] - Staining of human fallopian tube shows strong membranous positivity in glandular cells.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

NBP1-69082
Western Blot: BBS2 Antibody [NBP1-69082] - Titration: 1.0 ug/ml Positive Control: MCF7 Whole Cell.

Rabbit Polyclonal
Species Human, Mouse, Rat
Applications WB

1845-SH
1 μg/lane of Recombinant Human Sonic Hedgehog/Shh (C24II), N-Terminus was resolved with SDS-PAGE under reducing (R) conditions and visualized by silver staining, showing a single band at 22 kDa.MALDI-TOF analysis of Recombinant Human Sonic Hedgehog/Shh (C24II), N-Terminus. The major peak corresponds to the calculated molecular mass, 19814 Da. The minor peak at 20029  is a matrix-associated artifact of the MALDI-TOF.


Species Human

     5 Reviews

31 Publications
BC110-60480

Rabbit Polyclonal
Species Human, Mouse
Applications ICC/IF, PEP-ELISA

NBP2-78258


Species Human

NBP1-88969
Immunohistochemistry-Paraffin: B9D1 Antibody [NBP1-88969] - Staining of human liver shows strong cytoplasmic positivity with a granular pattern in hepatocytes.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

NBP1-84190
Immunohistochemistry-Paraffin: Nesprin 2 Antibody [NBP1-84190] - Staining of human colon.Immunohistochemistry-Paraffin: Nesprin 2 Antibody [NBP1-84190] - Staining of human cerebral cortex, colon, kidney and testis using Anti-SYNE2 antibody NBP1-84190 (A) shows similar protein distribution across tissues to independent antibody NBP2-38620 (B).

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

2 Publications
NBP2-47594
Immunocytochemistry/Immunofluorescence: TRIM26 Antibody [NBP2-47594] - Staining  human cell line A-431 shows positivity in cytoplasm and nucleus but excluded from the nucleoli.Immunohistochemistry-Paraffin: TRIM26 Antibody [NBP2-47594] - Staining of human tonsil shows strong cytoplasmic positivity in germinal center and non-germinal center cells.

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

NBP1-91693
Western Blot: B9D2 Antibody [NBP1-91693] - Analysis in control (vector only transfected HEK293T lysate) and B9D2 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).Immunohistochemistry-Paraffin: B9D2 Antibody [NBP1-91693] - Staining in human fallopian tube and skeletal muscle tissues using anti-B9D2 antibody. Corresponding B9D2 RNA-seq data are presented for the same tissues.

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

NBP1-87201
Western Blot: Prosurfactant Protein C Antibody [NBP1-87201] - Analysis in human lung tissue.Immunohistochemistry-Paraffin: Prosurfactant Protein C Antibody [NBP1-87201] -  Analysis in human lung and kidney tissues using HPA010928 antibody. Corresponding SFTPC RNA-seq data are presented for the same tissues.

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

NBP1-99477
Bioactivity: Recombinant Human PKC mu Protein [NBP1-99477] - Activity assessment, see Application Notes for more details.SDS-Page: Recombinant Human PKC mu Protein [NBP1-99477] - 1 ug of PKC mu protein. The scan of the gel showed >90% purity of the PKCmu product and the band was at ~131 kDa.


Species Human

NBP2-15309
Western Blot: AHI1 Antibody [NBP2-15309] - Sample (30 ug of whole cell lysate) A: IMR32 7.5% SDS PAGE; antibody diluted at 1:1000.Immunocytochemistry/Immunofluorescence: AHI1 Antibody [NBP2-15309] - Analysis of methanol-fixed HeLa, using antibody at 1:500 dilution.

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


Related Genes

Meckel-gruber Syndrome has been researched against:

Related PTMs

Meckel-gruber Syndrome has been studied in relation to posttranslational modifications (PTMs) including:

Alternate Names

Meckel-gruber Syndrome is also known as Dysencephalia Splachnocystica, Dysencephalia Splanchnocystica, Gruber Syndrome, Meckel Gruber Syndrome, Meckel Syndrome.