AGL Produits
(Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
Catégories
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. [provided by RefSeq, Jul 2008].
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Catégories AGL en vedette
AGL Anticorps
High quality antibodies with extensive validation data.
AGL Kits ELISA
Reliable ELISA kits for a wide range of species.
AGL Protéines
Proteins for various applications incl. WB, ELISA, IF etc.
AGL recommandé Anticorps
Produit
Reactivity
Application
Validations
N° du produit
Quantité
Fiche technique
Reactivity
Human
Application
WB, IF
Validations
- (6)
- (4)
N° du produit
ABIN389030
Quantité
400 μL
Fiche technique
Fiche technique
Reactivity
Human
Application
WB, IF
Validations
- (10)
- (2)
N° du produit
ABIN1882062
Quantité
400 μL
Fiche technique
Fiche technique
Reactivity
Human
Application
WB, ELISA, IF
Validations
- (1)
- (2)
N° du produit
ABIN545224
Quantité
400 μL
Fiche technique
Fiche technique
AGL recommandé Kits ELISA
Produit
Reactivity
Analytical Method
Validations
N° du produit
Quantité
Fiche technique
Reactivity
Human
Analytical Method
Quantitative Sandwich ELISA
Validations
- (1)
N° du produit
ABIN6953680
Quantité
96 tests
Fiche technique
Fiche technique
Reactivity
Human
Analytical Method
Sandwich ELISA
Validations
N° du produit
ABIN418882
Quantité
96 tests
Fiche technique
Fiche technique
Reactivity
Dog
Analytical Method
Validations
N° du produit
ABIN2870202
Quantité
96 tests
Fiche technique
Fiche technique
AGL recommandé Protéines
Produit
Reactivity
Source
Validations
N° du produit
Quantité
Fiche technique
Reactivity
Human
Source
Tobacco (Nicotiana tabacum)
Validations
- (1)
N° du produit
ABIN3092723
Quantité
1 mg
Fiche technique
Fiche technique
Reactivity
Mouse
Source
Escherichia coli (E. coli)
Validations
N° du produit
ABIN7422415
Quantité
100 μg
Fiche technique
Fiche technique
Reactivity
Human
Source
Escherichia coli (E. coli)
Validations
N° du produit
ABIN7420006
Quantité
100 μg
Fiche technique
Fiche technique
Dernières publications sur nos produits AGL
: "Commentary on: "Enzalutamide monotherapy in hormone-naive prostate cancer: primary analysis of an open-label, single-arm, phase 2 study." Tombal B, Borre M, Rathenborg P, Werbrouck P, Van Poppel H, ..." dans: Urologic oncology, (2015) (PubMed).: "Muscle glycogen remodeling and glycogen phosphate metabolism following exhaustive exercise of wild type and laforin knockout mice." dans: The Journal of biological chemistry, (2015) (PubMed).
: "Loss of glycogen debranching enzyme AGL drives bladder tumor growth via induction of hyaluronic acid synthesis." dans: Clinical cancer research : an official journal of the American Association for Cancer Research, (2015) (PubMed).
: "Laforin-malin complex degrades polyglucosan bodies in concert with glycogen debranching enzyme and brain isoform glycogen phosphorylase." dans: Molecular neurobiology, Vol. 49, Issue 2, pp. 645-57, (2014) (PubMed).
: "Anti-retinal antibodies in patients with macular telangiectasia type 2." dans: Investigative ophthalmology & visual science, Vol. 54, Issue 8, pp. 5675-83, (2013) (PubMed).
: "Genetic depletion of the malin E3 ubiquitin ligase in mice leads to lafora bodies and the accumulation of insoluble laforin." dans: The Journal of biological chemistry, Vol. 285, Issue 33, pp. 25372-81, (2010) (PubMed).
: "Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis." dans: Muscle & nerve, Vol. 39, Issue 6, pp. 739-53, (2009) (PubMed).
: "Abnormal metabolism of glycogen phosphate as a cause for Lafora disease." dans: The Journal of biological chemistry, Vol. 283, Issue 49, pp. 33816-25, (2008) (PubMed).
: "A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori's disease." dans: Genes & development, Vol. 21, Issue 19, pp. 2399-409, (2007) (PubMed).
: "Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III." dans: Journal of human genetics, Vol. 47, Issue 2, pp. 55-9, (2002) (PubMed).
Synonymes et noms alternatifs relatifs à AGL
amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (AGL), glycogen debranching enzyme (agl), glycogen debranching protein (MMAH_RS03870), amylo-1,6-glucosidase, 4-alpha-glucanotransferase (Agl), amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (Agl), 1110061O17Rik, 9430004C13Rik, 9630046L06Rik, AI850929, C77197, DDBDRAFT_0219237, DDBDRAFT_0234114, DDB_0219237, DDB_0234114, GDEProtein 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
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