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

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

list all antibodies Gene Name GeneID UniProt
ALG8 79053 Q9BVK2
ALG8 293129  
ALG8 381903 Q6P8H8
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Top anti-ALG8 Antibodies at antibodies-online.com

Showing 10 out of 34 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Cow Rabbit Un-conjugated WB 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Mouse Un-conjugated ELISA, WB Detection limit for recombinant GST tagged ALG8 is approximately 0.3 ng/mL as a capture antibody. 0.1 mg Log in to see 8 to 11 Days
$450.00
Details
Bat Rabbit Un-conjugated WB 50 μg Log in to see 7 to 9 Days
$551.83
Details
Human Rabbit Un-conjugated WB ALG8 Antibody (N-term)  western blot analysis in MDA-MB453 cell line lysates (35ug/lane).This demonstrates the ALG8 antibody detected the ALG8 protein (arrow). 400 μL Log in to see 10 to 11 Days
$324.50
Details
Human Mouse Un-conjugated ELISA, WB Detection limit for recombinant GST tagged ALG8 is approximately 0.3ng/ml as a capture antibody. Western Blot detection against Immunogen (33.99 KDa) . 100 μg Log in to see 11 to 12 Days
$430.00
Details
Rat Rabbit Un-conjugated WB Western Blot: ALG8 Antibody [NBP1-69028] - Rat Heart lysate, concentration 0.2-1 ug/ml. 100 μL Log in to see 8 to 11 Days
$447.56
Details
Human Rabbit Un-conjugated ICC, IF, IHC, IHC (p), WB Immunohistochemistry: ALG8 Antibody [NBP2-47550] - Analysis of human colon tissue. Shows strong granular cytoplasmic positivity in glandular cells. Immunocytochemistry/Immunofluorescence: ALG8 Antibody [NBP2-47550] - Analysis of human cell line A-431 shows positivity in nucleus but excluded from the nucleoli. 0.1 mL Log in to see 10 to 13 Days
$439.69
Details
Human Rabbit Un-conjugated ELISA, WB   200 μL Log in to see 7 to 9 Days
$793.83
Details
Human Rabbit PE ELISA, WB   200 μL Log in to see 7 to 9 Days
$1,013.83
Details
Human Rabbit Alkaline Phosphatase (AP) ELISA, WB   200 μL Log in to see 7 to 9 Days
$1,013.83
Details

ALG8 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human ,
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Rat (Rattus) ,


Mouse (Murine) ,


More Antibodies against 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 Antibodies) and SEC63 (show SEC63 Antibodies), to identify heterozygous loss-of-function mutations in 3 additional genes, ALG8, GANAB (show GANAB Antibodies), and SEC61B (show SEC61B Antibodies). Similarly to PRKCSH (show PRKCSH Antibodies) and SEC63 (show SEC63 Antibodies), 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 Antibodies) 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

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) antibody
  • ALG8, alpha-1,3-glucosyltransferase (Alg8) antibody
  • asparagine-linked glycosylation 8 (alpha-1,3-glucosyltransferase) (Alg8) antibody
  • asparagine-linked glycosylation 8, alpha-1,3-glucosyltransferase homolog (S. cerevisiae) (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

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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