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

ALG8 encodes a member of the ALG6/ALG8 glucosyltransferase family. Additionally we are shipping ALG8 Antibodies (33) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
ALG8 79053 Q9BVK2
Rat ALG8 ALG8 293129  
ALG8 381903 Q6P8H8
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Top ALG8 Proteins at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 49 to 54 Days
$6,041.49
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 49 to 54 Days
$4,244.78
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details

ALG8 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine)

More Proteins for Asparagine-Linked Glycosylation 8, alpha-1,3-Glucosyltransferase Homolog (S. Cerevisiae) (ALG8) Interaction Partners

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

  1. In ALG8-CDG, isoelectric focusing of transferrin (show Tf Proteins) 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

  2. 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.

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

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

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

ALG8 Protein Profile

Protein 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)
  • ALG8, alpha-1,3-glucosyltransferase (Alg8)
  • asparagine-linked glycosylation 8 (alpha-1,3-glucosyltransferase) (Alg8)
  • asparagine-linked glycosylation 8, alpha-1,3-glucosyltransferase homolog (S. cerevisiae) (ALG8)
  • AI447372 protein
  • CDG1H protein
  • Gm1089 protein

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

GENE ID SPECIES
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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