AGL Antibodies
Choose one of 39 AGL antibodies from our product listing based on 16 publications and 17 validation images.
Explore reliable AGL antibodies from a broad selection of renowned manufacturers. Our portfolio enables accurate AGL detection across multiple species, including Human, Mouse, Rat, and supports diverse research applications such as IF, WB, ELISA, ICC, IHC.
Quickly find the right antibody using our search, filter, and comparison tools. Each product page provides detailed validation data, literature references, and customer feedback. Unlike comparison-only resources, you can conveniently purchase antibodies directly through our site. Choose from polyclonal, monoclonal, or recombinant AGL antibodies derived from various hosts such as Rabbit, Mouse. Browse our products below and order directly to support your research with confidence.
Alternative names for AGL are AGL, agl, MMAH_RS03870, Agl.
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39 results
Latest Publications for our AGL Antibodies
: "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, ..." in: Urologic oncology, (2015) (PubMed).: "Muscle glycogen remodeling and glycogen phosphate metabolism following exhaustive exercise of wild type and laforin knockout mice." in: The Journal of biological chemistry, (2015) (PubMed).
: "Loss of glycogen debranching enzyme AGL drives bladder tumor growth via induction of hyaluronic acid synthesis." in: 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." in: Molecular neurobiology, Vol. 49, Issue 2, pp. 645-57, (2014) (PubMed).
: "Anti-retinal antibodies in patients with macular telangiectasia type 2." in: 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." in: 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." in: Muscle & nerve, Vol. 39, Issue 6, pp. 739-53, (2009) (PubMed).
: "Abnormal metabolism of glycogen phosphate as a cause for Lafora disease." in: 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." in: 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." in: Journal of human genetics, Vol. 47, Issue 2, pp. 55-9, (2002) (PubMed).
Aliases for AGL Antibodies
amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (AGL) Antibodiesglycogen debranching enzyme (agl) Antibodies
glycogen debranching protein (MMAH_RS03870) Antibodies
amylo-1,6-glucosidase, 4-alpha-glucanotransferase (Agl) Antibodies
amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (Agl) Antibodies
1110061O17Rik Antibodies
9430004C13Rik Antibodies
9630046L06Rik Antibodies
AI850929 Antibodies
C77197 Antibodies
DDBDRAFT_0219237 Antibodies
DDBDRAFT_0234114 Antibodies
DDB_0219237 Antibodies
DDB_0234114 Antibodies
GDE Antibodies
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