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Congenital Disorders Of Glycosylation: Disease Bioinformatics

Research of Congenital Disorders Of Glycosylation has been linked to Congenital Disorders, Metabolic Diseases, Carbohydrate-deficient Glycoprotein Syndrome Type , Muscle Hypotonia, Atrophy. The study of Congenital Disorders Of Glycosylation has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Congenital Disorders Of Glycosylation include Glycosylation, Protein Glycosylation, Transport, Coagulation, Pathogenesis. These pathways complement our catalog of research reagents for the study of Congenital Disorders Of Glycosylation including antibodies and ELISA kits against TF, PMM2, MPI, PHOSPHOMANNOSE ISOMERASE, STRABISMUS.

Congenital Disorders Of Glycosylation 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 Disorders Of Glycosylation below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 560 products for the study of Congenital Disorders Of Glycosylation that can be applied to Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

NB600-610
Immunohistochemistry-Paraffin: Apolipoprotein CIII Antibody [NB600-610] - Tissue: liver.

Goat Polyclonal
Species Human, Bovine
Applications WB, ELISA, IHC

     1 Review

2 Publications
NBP1-62494
Western Blot: ALG6 Antibody [NBP1-62494] - Human Fetal Heart, Antibody Dilution: 1.0 ug/ml.Western Blot: ALG6 Antibody [NBP1-62494] - Hela cell lysate, concentration 0.2-1 ug/ml.

Rabbit Polyclonal
Species Human
Applications WB

NBP1-81414
Western Blot: COG1 Antibody [NBP1-81414] - Lane 1: Marker  [kDa] 230, 130, 95, 72, 56, 36, 28, 17, 11.  Lane 2: Human cell line RT-131Immunohistochemistry-Paraffin: COG1 Antibody [NBP1-81414] - Staining of human placenta shows strong cytoplasmic positivity in trophoblastic cells.

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

NBP1-87055
Western Blot: PMM1/Phosphomannomutase 1 Antibody [NBP1-87055] - Lane 1: NIH-3T3 cell lysate (Mouse embryonic fibroblast cells). Lane 2: NBT-II cell lysate (Rat Wistar bladder tumor cells).Immunohistochemistry-Paraffin: PMM1/Phosphomannomutase 1 Antibody [NBP1-87055] - Staining of human pancreas shows moderate nuclear positivity in exocrine glandular cells.

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

NBP2-02043
Western Blot: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Mannose Phosphate Isomerase (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-Mannose Phosphate Isomerase.Immunocytochemistry/Immunofluorescence: Mannose Phosphate Isomerase Antibody (1C7) [NBP2-02043] Staining of COS7 cells transiently transfected by pCMV6-ENTRY Mannose Phosphate Isomerase.

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

NBP2-14868
Western Blot: Dystroglycan Antibody [NBP2-14868] - Various tissue extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Dystroglycan Antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.Immunocytochemistry/Immunofluorescence: Dystroglycan Antibody [NBP2-14868] - HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: Dystroglycan protein stained by Dystroglycan antibody 38) diluted at 1:1000. Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [B-5-1-2]  diluted at 1:10000. Blue: Hoechst 33342 staining.

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

2 Publications
NBP2-32539
Immunocytochemistry/Immunofluorescence: ALG1 Antibody [NBP2-32539] - Staining of human cell line Hep G2 shows localization to nucleoli fibrillar center & endoplasmic reticulum.Immunohistochemistry-Paraffin: ALG1 Antibody [NBP2-32539] - Staining of human testis shows strong cytoplasmic positivity in cells in seminiferus ducts, Leydig cells shows moderate staining.

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

2914-HT


Species Human
Applications BA

     2 Reviews

25 Publications
DPI00
 SLPI [HRP] SLPI [HRP]


Species Human
Applications ELISA

29 Publications
NBP2-57753
Western Blot: PMM2/Phosphomannomutase 2 Antibody [NBP2-57753] - Western blot analysis in human cell line RT-4, human cell line U-251 MG, human plasma, human liver tissue and human tonsil tissue.Immunocytochemistry/Immunofluorescence: PMM2/Phosphomannomutase 2 Antibody [NBP2-57753] - Staining of human cell line SH-SY5Y shows localization to nucleus & cytosol.

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

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

NBP1-05034
Western Blot: DPM1 Antibody [NBP1-05034] - (0.1ug/ml) staining of Human Liver lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.Immunohistochemistry-Paraffin: DPM1 Antibody [NBP1-05034] - (3.75ug/ml) staining of paraffin embedded Human Tonsil. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.

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

1 Publication
NBP2-80392
Western Blot: Serpin C1/Antithrombin-III Antibody (15F1) [NBP2-80392] - Analysis of SERPINC1 on zebrafish tissue lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:5,000 dilution was used for 1 hour at room temperature.Immunohistochemistry-Paraffin: Serpin C1/Antithrombin-III Antibody (15F1) [NBP2-80392] - Analysis in mouse kidney tissue using Serpin C1/Antithrombin-III antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room tempe

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, Flow, IHC

NBP1-05032
Western Blot: COG7 Antibody [NBP1-05032] - (0.03ug/ml) staining of MOLT4 lysate (35ug protein in RIPA buffer). Detected by chemiluminescence.Immunohistochemistry-Paraffin: COG7 Antibody [NBP1-05032] - (5ug/ml) staining of paraffin embedded Human Testis. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.

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

1 Publication
NBP2-93465
Western Blot: TMEM11 Antibody [NBP2-93465] - Analysis of extracts of HeLa cells, using TMEM11 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:Immunocytochemistry/Immunofluorescence: TMEM11 Antibody [NBP2-93465] - Analysis of L929 cells using TMEM11 at dilution of 1:100. Blue: DAPI for nuclear staining.

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

H00005555-P01
SDS-Page: Recombinant Human PRH2 Protein [H00005555-P01] - 12.5% SDS-PAGE Stained with Coomassie Blue.


Species Human
Applications WB, ELISA, PA

10711-GT
Lane 1 contained substrate glycan M1N1f' (<a class=NoLineLink href=https://www.rndsystems.com/search?keywords=GL302>GL302</a>). In the presence of rhMGAT2, the glycan was modified and a mobility shift was observed.MGAT2 (Catalog # 10711-GT) recognizes an unmodified GlcNAc residue installed by MGAT1 (<a class=NoLineLink href=


Species Human
Applications EnzAct


Related Genes

Congenital Disorders Of Glycosylation has been researched against:

Related PTMs

Congenital Disorders Of Glycosylation has been studied in relation to posttranslational modifications (PTMs) including:

Alternate Names

Congenital Disorders Of Glycosylation is also known as Carbohydrate Deficient Glycoprotein Syndrome, Carbohydrate-deficient Glycoprotein Syndrome, Carbohydrate-deficient Glycoprotein Syndromes.