Browse our anti-AGL (AGL) Antibodies

Full name:
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase Antibodies (AGL)
On are 46 Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) Antibodies from 12 different suppliers available. Additionally we are shipping AGL Proteins (5) and AGL Kits (3) and many more products for this protein. A total of 58 AGL products are currently listed.
1110061O17Rik, 9430004C13Rik, 9630046L06Rik, AI850929, C77197, DDBDRAFT_0219237, DDBDRAFT_0234114, DDB_0219237, DDB_0234114, GDE
list all antibodies Gene Name GeneID UniProt
AGL 77559  
AGL 178 P35573
AGL 362029  

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Most Popular Reactivities for anti-AGL (AGL) Antibodies

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anti-Mouse (Murine) AGL Antibodies:

anti-Human AGL Antibodies:

anti-Rat (Rattus) AGL Antibodies:

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Top referenced anti-AGL Antibodies

  1. Human Polyclonal AGL Primary Antibody for IF, WB - ABIN1882062 : Hansen, Lundin, Markussen, Thorsby: T cell receptor usage by HLA-DQw8-specific T cell clones. in International immunology 1992 (PubMed)
    Show all 10 references for 1882062

  2. Human Polyclonal AGL Primary Antibody for IF, WB - ABIN389030 : Parker, Kong, Walsh, Salajegheh, Moghadaszadeh, Amato, Nazareno, Lin, Krastins, Sarracino, Beggs, Pinkus, Greenberg: Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis. in Muscle & nerve 2009 (PubMed)
    Show all 9 references for 389030

  3. Human Polyclonal AGL Primary Antibody for IP, WB - ABIN343185 : Parker, Koay, Gilbert-Wilson, Waddington, Stapleton: AMP-activated protein kinase does not associate with glycogen alpha-particles from rat liver. in Biochemical and biophysical research communications 2007 (PubMed)
    Show all 3 references for 343185

  4. Human Polyclonal AGL Primary Antibody for EIA, IF - ABIN357688 : Horinishi, Okubo, Tang, Hui, To, Mabuchi, Okada, Mabuchi, Murase: Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III. in Journal of human genetics 2002 (PubMed)
    Show all 2 references for 357688

More Antibodies against AGL Interaction Partners

Human Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) interaction partners

  1. The study identified 31 novel mutations and extended the mutation spectrum of AGL in Chinese patients with glycogen (show GYS1 Antibodies) storage disease type III.

  2. Our study establishes HAS2 (show HAS2 Antibodies)-mediated HA synthesis as a driver of growth of bladder cancer with low AGL and provides preclinical rationale for personalized targeting of HAS2 (show HAS2 Antibodies)/HA signaling in patients with low amylo-alpha-1-6-glucosidase-4-alpha-glucanotransferase -expressing tumors.

  3. AGL loss causes high SHMT2 (show SHMT2 Antibodies) expression and consequently increases glycine-dependent nucleotide synthesis leading to bladder cancer growth.

  4. Point mutations in AGL gene are associated with glycogen (show GYS1 Antibodies) storage disease type IIIa in a Chinese family.

  5. AGL haplotype analyses suggested that c.1019delA and c.958+1G>A are founder mutations in Turkish patients, while p.R864X is a recurrent mutation.

  6. A homozygous frameshift deletion, c.4456delT, in exon 33 of the AGL gene in Inuit children determines the cause of glycogen (show GYS1 Antibodies) storage disease type IIIa and confirms a founder effect.

  7. study identified 10 different mutations in 8 Korean Glycogen (show GYS1 Antibodies) storage disease type III patients; 5 mutations are novel and include 1 nonsense (c.1461G>A, p.W487X), 3 splicing (c.293+4_293+6delAGT in IVS4, c.460+1G>T in IVS5, c.2682-8A>G in IVS21) and 1 missense mutation (c.2591G>C, p.R864P)

  8. Characterization of a novel homozygous single point mutation at the polypyrimidine tract of intron 21 of the AGL gene in two consanguineous siblings with glycogen (show GYS1 Antibodies) storage disease type III.

  9. We found that most patients with macular telangiectasia-2 possess retinal autoantibodies, the most prevalent of which were directed against AGL, RBP3 (show E2F1 Antibodies), and CK-B.

  10. A founder effect discovered amongst Tunisian patients with glycogen (show GYS1 Antibodies) storage disease type III and a c.3216_3217delGA mutation in the AGL gene.

AGL Antigen Profile

Antigen Summary

This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described.

Alternative names and synonyms associated with AGL

  • amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (AGL) antibody
  • glycogen debranching enzyme (agl) antibody
  • glycogen debranching enzyme (Mmah_0764) antibody
  • amylo-1,6-glucosidase, 4-alpha-glucanotransferase (Agl) antibody
  • amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (Agl) antibody
  • 1110061O17Rik antibody
  • 9430004C13Rik antibody
  • 9630046L06Rik antibody
  • AI850929 antibody
  • C77197 antibody
  • DDBDRAFT_0219237 antibody
  • DDBDRAFT_0234114 antibody
  • DDB_0219237 antibody
  • DDB_0234114 antibody
  • GDE antibody

Protein level used designations for AGL

amylo-1, 6-glucosidase, 4-alpha-glucanotransferase (glycogen debranching enzyme, glycogen storage disease type III) , glycogen debranching enzyme , amylo-1, 6-glucosidase, 4-alpha-glucanotransferase , amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase , glycogen storage disease type III , glycogen debrancher , amylo-1,6-glucosidase, 4-alpha-glucanotransferase , Glycogen debrancher

469392 Pan troglodytes
517397 Bos taurus
8626162 Dictyostelium discoideum AX4
8982925 Methanohalophilus mahii DSM 5219
100126856 Sus scrofa
77559 Mus musculus
178 Homo sapiens
362029 Rattus norvegicus
479931 Canis lupus familiaris
100050695 Equus caballus
100009066 Oryctolagus cuniculus
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