AGL 抗体
(Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
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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41 results :
AGL
适用: 人
WB, IF
宿主: 兔
Polyclonal
RB4978
unconjugated
6 references
AGL
适用: 人
WB, IF
宿主: 兔
Polyclonal
RB4976
unconjugated
10 references
KD Validated
AGL
适用: 人, 小鼠, 大鼠
WB, IF, IHC, ICC, FACS
宿主: 兔
Monoclonal
unconjugated
Recombinant Antibody
Latest Publications for our AGL 抗体
: "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 抗体
amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (AGL) 抗体glycogen debranching enzyme (agl) 抗体
glycogen debranching protein (MMAH_RS03870) 抗体
amylo-1,6-glucosidase, 4-alpha-glucanotransferase (Agl) 抗体
amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase (Agl) 抗体
1110061O17Rik 抗体
9430004C13Rik 抗体
9630046L06Rik 抗体
AI850929 抗体
C77197 抗体
DDBDRAFT_0219237 抗体
DDBDRAFT_0234114 抗体
DDB_0219237 抗体
DDB_0234114 抗体
GDE 抗体
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