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- References [8]
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- Product number
- ABIN563505 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Epilepsy, Progressive Myoclonus Type 2A, Lafora Disease (Laforin) (EPM2A) (AA 101-199), (partial) antibody
- Antibody type
- Monoclonal
- Reactivity
- Human
- Host
- Mouse
- Epitope
- AA 101-199, partial
- Isotype
- IgG
- Antibody clone number
- 6C6
- Vial size
- 100 μg
- Storage
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Handling
- Aliquot to avoid repeated freezing and thawing.
Submitted references Muscle glycogen remodeling and glycogen phosphate metabolism following exhaustive exercise of wild type and laforin knockout mice.
The carbohydrate-binding domain of overexpressed STBD1 is important for its stability and protein-protein interactions.
A bioassay for Lafora disease and laforin glucan phosphatase activity.
Early-onset Lafora body disease.
Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora disease.
Laforin and malin knockout mice have normal glucose disposal and insulin sensitivity.
Glycogen hyperphosphorylation underlies lafora body formation.
Laforin is a glycogen phosphatase, deficiency of which leads to elevated phosphorylation of glycogen in vivo.
Irimia JM, Tagliabracci VS, Meyer CM, Segvich DM, DePaoli-Roach AA, Roach PJ
The Journal of biological chemistry 2015 Sep 11;290(37):22686-98
The Journal of biological chemistry 2015 Sep 11;290(37):22686-98
The carbohydrate-binding domain of overexpressed STBD1 is important for its stability and protein-protein interactions.
Zhu Y, Zhang M, Kelly AR, Cheng A
Bioscience reports 2014 Jul 1;34(4)
Bioscience reports 2014 Jul 1;34(4)
A bioassay for Lafora disease and laforin glucan phosphatase activity.
Sherwood AR, Johnson MB, Delgado-Escueta AV, Gentry MS
Clinical biochemistry 2013 Dec;46(18):1869-76
Clinical biochemistry 2013 Dec;46(18):1869-76
Early-onset Lafora body disease.
Turnbull J, Girard JM, Lohi H, Chan EM, Wang P, Tiberia E, Omer S, Ahmed M, Bennett C, Chakrabarty A, Tyagi A, Liu Y, Pencea N, Zhao X, Scherer SW, Ackerley CA, Minassian BA
Brain : a journal of neurology 2012 Sep;135(Pt 9):2684-98
Brain : a journal of neurology 2012 Sep;135(Pt 9):2684-98
Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora disease.
Tiberia E, Turnbull J, Wang T, Ruggieri A, Zhao XC, Pencea N, Israelian J, Wang Y, Ackerley CA, Wang P, Liu Y, Minassian BA
The Journal of biological chemistry 2012 Jul 20;287(30):25650-9
The Journal of biological chemistry 2012 Jul 20;287(30):25650-9
Laforin and malin knockout mice have normal glucose disposal and insulin sensitivity.
DePaoli-Roach AA, Segvich DM, Meyer CM, Rahimi Y, Worby CA, Gentry MS, Roach PJ
Human molecular genetics 2012 Apr 1;21(7):1604-10
Human molecular genetics 2012 Apr 1;21(7):1604-10
Glycogen hyperphosphorylation underlies lafora body formation.
Turnbull J, Wang P, Girard JM, Ruggieri A, Wang TJ, Draginov AG, Kameka AP, Pencea N, Zhao X, Ackerley CA, Minassian BA
Annals of neurology 2010 Dec;68(6):925-33
Annals of neurology 2010 Dec;68(6):925-33
Laforin is a glycogen phosphatase, deficiency of which leads to elevated phosphorylation of glycogen in vivo.
Tagliabracci VS, Turnbull J, Wang W, Girard JM, Zhao X, Skurat AV, Delgado-Escueta AV, Minassian BA, Depaoli-Roach AA, Roach PJ
Proceedings of the National Academy of Sciences of the United States of America 2007 Dec 4;104(49):19262-6
Proceedings of the National Academy of Sciences of the United States of America 2007 Dec 4;104(49):19262-6
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Supportive validation
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- antibodies-online (provider)
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- Experimental details
- WB
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- ELISA
