Asparagine-Linked Glycosylation 8, alpha-1,3-Glucosyltransferase Homolog (S. Cerevisiae) (ALG8) ELISA Kits

ALG8 encodes a member of the ALG6/ALG8 glucosyltransferase family. Additionally we are shipping ALG8 Antibodies (34) and ALG8 Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human ALG8 ALG8 79053 Q9BVK2
Anti-Rat ALG8 ALG8 293129  
Anti-Mouse ALG8 ALG8 381903 Q6P8H8
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More ELISA Kits for ALG8 Interaction Partners

Human Asparagine-Linked Glycosylation 8, alpha-1,3-Glucosyltransferase Homolog (S. Cerevisiae) (ALG8) interaction partners

  1. used whole exome sequencing in a discovery cohort of 102 unrelated patients who were excluded for mutations in the 2 most common polycystic liver disease genes, PRKCSH (show PRKCSH ELISA Kits) and SEC63 (show SEC63 ELISA Kits), to identify heterozygous loss-of-function mutations in 3 additional genes, ALG8, GANAB (show GANAB ELISA Kits), and SEC61B (show SEC61B ELISA Kits). Similarly to PRKCSH (show PRKCSH ELISA Kits) and SEC63 (show SEC63 ELISA Kits), these genes encode proteins that are integral to the protein biogenesis pathway in the endoplasmic reticulum.

  2. In ALG8-CDG, isoelectric focusing of transferrin (show Tf ELISA Kits) in serum or plasma shows an abnormal sialotransferrin pattern. The diagnosis is confirmed by mutation analysis in ALG8; all patients reported so far had point mutations or small deletions

  3. We reviewed the clinical features in all nine previously reported patients diagnosed with ALG8-disorder of glycosylation with a special focus on their skin signs.

  4. Severe ALG8 congenital disorder of glycosylation(CDG-Ih) is associated with homozygosity for two novel missense mutations in exon 8 of ALG8

  5. ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih.

  6. ALG8 splice site mutations and missense mutations causing ALG8 deficiency in patients with congenital disorders of glycosylation type Ih.

ALG8 Antigen Profile

Antigen Summary

This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition of the second glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation of proteins. Mutations in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ih). Alternatively spliced transcript variants encoding different isoforms have been identified.

Gene names and symbols associated with ALG8

  • ALG8, alpha-1,3-glucosyltransferase (ALG8) antibody
  • ALG8, alpha-1,3-glucosyltransferase (Alg8) antibody
  • asparagine-linked glycosylation 8 (alpha-1,3-glucosyltransferase) (Alg8) antibody
  • AI447372 antibody
  • CDG1H antibody
  • Gm1089 antibody

Protein level used designations for ALG8

HUSSY-02 , asparagine-linked glycosylation 8 homolog (S. cerevisiae, alpha-1,3-glucosyltransferase) , asparagine-linked glycosylation 8 homolog (yeast, alpha-1,3-glucosyltransferase) , asparagine-linked glycosylation 8, alpha-1,3-glucosyltransferase homolog , asparagine-linked glycosylation protein 8 homolog , dol-P-Glc:Glc(1)Man(9)GlcNAc(2)-PP-dolichyl alpha-1,3-glucosyltransferase , dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase , dolichyl-P-Glc:Glc(1)Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase , dolichyl-P-Glc:Glc1Man9GlcNAc2-PP-dolichyl glucosyltransferase , dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl-alpha-1,3-glucosyltransferase , probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase

79053 Homo sapiens
293129 Rattus norvegicus
381903 Mus musculus
538731 Bos taurus
428097 Gallus gallus
476793 Canis lupus familiaris
100511030 Sus scrofa
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