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Congenital Disorder Of Glycosylation, Type 2c: Disease Bioinformatics

Research of Congenital Disorder Of Glycosylation, Type 2c has been linked to Leukocyte-adhesion Deficiency Syndrome, Tissue Adhesions, Leukocyte Adhesion Deficiency, Infective Disorder, Fetal Diseases. The study of Congenital Disorder Of Glycosylation, Type 2c has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Congenital Disorder Of Glycosylation, Type 2c include Transport, Fucosylation. These pathways complement our catalog of research reagents for the study of Congenital Disorder Of Glycosylation, Type 2c including antibodies and ELISA kits against SLC35C1, SELP, ATN1, SELE, FUT1.

Congenital Disorder Of Glycosylation, Type 2c 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 Disorder Of Glycosylation, Type 2c below! For more information on how to use Laverne, please read the How to Guide.
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Top Research Reagents

We have 430 products for the study of Congenital Disorder Of Glycosylation, Type 2c that can be applied to Western Blot, Flow Cytometry, Immunohistochemistry, Immunocytochemistry/Immunofluorescence from our catalog of antibodies and ELISA kits.

NBP2-49410
Immunocytochemistry/Immunofluorescence: SLC35C1 Antibody [NBP2-49410] - Immunofluorescent staining of human cell line A549 shows localization to the Golgi apparatus.Immunohistochemistry-Paraffin: SLC35C1 Antibody [NBP2-49410] - Staining in human small intestine and kidney tissues using anti-SLC35C1 antibody. Corresponding SLC35C1 RNA-seq data are presented for the same tissues.

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

137-PS


Species Human

     4 Reviews

33 Publications
NBP1-90044
Immunocytochemistry/Immunofluorescence: ATN1 Antibody [NBP1-90044] - Staining of human cell line U-251 MG shows localization to nucleoplasm. Antibody staining is shown in green.Immunohistochemistry-Paraffin: ATN1 Antibody [NBP1-90044] - Staining of human liver shows no positivity in hepatocytes as expected.

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

1 Publication
BBA16
<P align=left>E‑Selectin/CD62E was detected in immersion fixed paraffin-embedded sections of human brain (occipital cortex) using 10 µg/mL Mouse Anti-Human E‑Selectin/CD62E Monoclonal Antibody (Catalog # BBA16) 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=<P align=left>E-Selectin/CD62E was detected in immersion fixed HUVEC human umbilical vein endothelial cells activated with TNF‑ alpha  (Catalog # <A class=NoLineLink href=

Mouse Monoclonal
Species Human
Applications WB, IHC, IP

     1 Review

39 Publications
NBP1-57016
Western Blot: Blood group H inhibitor Antibody [NBP1-57016] - Human Heart lysate, concentration 0.2-1 ug/ml.

Rabbit Polyclonal
Species Human
Applications WB

AF1916
p63/TP73L was detected in immersion fixed paraffin-embedded sections of human breast using Goat Anti-Human p63/TP73L Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1916) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # <A class=NoLineLink href=p63/TP73L was detected in immersion fixed SCC-25 human tongue carcinoma cell line using Goat Anti-Human p63/TP73L Antigen Affinity-purified Polyclonal Antibody (Catalog # AF1916) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Goat IgG Secondary Antibody (yellow; Catalog # <A class=NoLineLink href=

Goat Polyclonal
Species Human
Applications WB, IHC, ICC

     3 Reviews

3 Publications

Related Genes

Congenital Disorder Of Glycosylation, Type 2c has been researched against:

Related Pathways

Congenital Disorder Of Glycosylation, Type 2c has been linked to:

Alternate Names

Congenital Disorder Of Glycosylation, Type 2c is also known as Leukocyte Adhesion Deficiency Type 2.