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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 PHOSPHOMANNOSE ISOMERASE, STRABISMUS, IA, APOC3, SERPINC1.

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

NB500-418
Western Blot: Transferrin Antibody (HTF-14) [NB500-418] - Analysis using the Azide Free version of NB500-418. Detection of 1. hTransferrin; 5 ug/well (red. con.) 2. hTransferrin; 3 ug/well (red. con.) 3. hTransferrin; 1 ug/well (red. con.) M. Low Range marker 4. hTransferrin; 1 ug/well (non-red. con.) 5. hTransferrin; 3 ug/well (non-red. con.)  6. hTransferrin; 5 ug/well (non-red. con.)

Mouse Monoclonal
Species Human, Porcine, Rabbit
Applications WB, B/N, ELISA

     1 Review

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

NBP2-02043
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
Applications WB, Flow, ICC/IF

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
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

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

NBP2-13443
Western Blot: TMEM11 Antibody [NBP2-13443] - 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 spImmunohistochemistry-Paraffin: TMEM11 Antibody [NBP2-13443] - Staining of human lymph node shows strong positivity in a subset of leukocytes.

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

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

Goat Polyclonal
Species Human
Applications WB, ELISA, IHC

     1 Review

1 Publication
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

MAB1287

Rat Monoclonal
Species Mouse
Applications WB

3 Publications
NBP2-47502
Western Blot: COG7 Antibody [NBP2-47502] - Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10. Lane 2: Negative control (vector only transfected HEK293T lysate). Lane 3: Over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).Immunocytochemistry/Immunofluorescence: COG7 Antibody [NBP2-47502] - Immunofluorescent staining of human cell line A-431 shows localization to the Golgi apparatus.

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

H00005555-P01
12.5% SDS-PAGE Stained with Coomassie Blue.


Species Human

NBP2-14235
Western Blot: MGAT2 Antibody [NBP2-14235] - Lane 1: Marker  [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10.  Lane 2: Human cell line RT-4Immunohistochemistry-Paraffin: MGAT2 Antibody [NBP2-14235] - Staining of human stomach, lower shows strong cytoplasmic positivity in glandular cells.

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

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

AF6868
Western blot shows lysates of MCF‑7 human breast cancer cell line, SH‑SY5Y human neuroblastoma cell line, human muscle tissue, and human placenta tissue. PVDF membrane was probed with 1 µg/mL of Sheep Anti-Human Dystroglycan Antigen Affinity-purified Polyclonal Antibody (Catalog # AF6868) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # <A class=NoLineLink href=Dystroglycan was detected in immersion fixed paraffin-embedded sections of human skeletal muscle using Sheep Anti-Human Dystroglycan Antigen Affinity-purified Polyclonal Antibody (Catalog # AF6868) at 3 µg/mL overnight at 4 °C. Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent-Basic (Catalog # <A class=NoLineLink href=

Sheep Polyclonal
Species Human
Applications WB, IHC

1 Publication
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


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.