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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.

Top Research Reagents

We have 1122 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.

NBP3-15543
Western Blot: COG1 Antibody [NBP3-15543] - Western blot analysis of extracts of 22Rv1 cells, using COG1 Rabbit pAb (NBP3-15543) 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: 90s.Immunohistochemistry-Paraffin: COG1 Antibody [NBP3-15543] - Immunohistochemistry of paraffin-embedded Human colon using COG1 Rabbit pAb (NBP3-15543) at dilution of 1:50 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.

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

NB600-610
Immunohistochemistry-Paraffin: Apolipoprotein CIII Antibody [NB600-610] - Tissue: liver.Immunohistochemistry of Apolipoprotein CIII Antibody.  Tissue: human liver.  Fixation: formalin fixed paraffin embedded.  Antigen retrieval: not required. Primary antibody: Apolipoprotein C-III at 2.5 ug/mL for 1 h at RT. Secondary antibody: Peroxidase goat secondary antibody at 1:10,000 for 45 min at RT. Staining: Apolipoprotein C-III as precipitated red signal with hematoxylin purple nuclear counterstain.

Goat Polyclonal
Species Human, Bovine
Applications WB, ELISA, ICC/IF

     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

NBP1-87055
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

NBP2-32539
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

AF1267

Goat Polyclonal
Species Human
Applications WB, IP, Neut

6 Publications
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=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=

Sheep Polyclonal
Species Human
Applications WB, IHC, KO

23 Publications
DHAPG0
N/A Haptoglobin [HRP]N/A Haptoglobin [HRP]


Species Human
Applications ELISA

7 Publications
2914-HT


Species Human
Applications BA

51 Publications
DPI00
N/A SLPI [HRP]N/A SLPI [HRP]


Species Human
Applications ELISA

37 Publications
NBP2-57753
PMM2/Phosphomannomutase 2 Antibody [NBP2-57753] - Western blot -Analysis using Anti-PMM2 antibody NBP2-57753 (A) shows similar pattern to independent antibody (B).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

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
NBP1-05032
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
MGAT2 (Catalog # 10711-GT) recognizes an unmodified GlcNAc residue installed by MGAT1 (<a class=NoLineLink href=1 μg/lane of Recombinant Human MGAT2 His-tag (Catalog # 10711-GT) was resolved with SDS-PAGE under reducing (R) conditions and visualized by silver staining, showing bands at 46-54 kDa.


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.