Antibody data
- Antibody Data
- Antigen structure
- References [6]
- Comments [0]
- Validations
- Western blot [2]
- ELISA [1]
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- Product number
- ABIN561206 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Glycogenin 1 (GYG1) (AA 1-73), (partial) antibody
- Antibody type
- Monoclonal
- Reactivity
- Human
- Host
- Mouse
- Epitope
- AA 1-73, partial
- Isotype
- IgG
- Antibody clone number
- 3B5
- 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 Cardiomyopathy as presenting sign of glycogenin-1 deficiency-report of three cases and review of the literature.
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods.
LC-MS/MS characterization of combined glycogenin-1 and glycogenin-2 enzymatic activities reveals their self-glucosylation preferences.
A new muscle glycogen storage disease associated with glycogenin-1 deficiency.
Dysregulation of multiple facets of glycogen metabolism in a murine model of Pompe disease.
Molecular pathogenesis of a new glycogenosis caused by a glycogenin-1 mutation.
Hedberg-Oldfors C, Glamuzina E, Ruygrok P, Anderson LJ, Elliott P, Watkinson O, Occleshaw C, Abernathy M, Turner C, Kingston N, Murphy E, Oldfors A
Journal of inherited metabolic disease 2017 Jan;40(1):139-149
Journal of inherited metabolic disease 2017 Jan;40(1):139-149
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods.
Tasca G, Fattori F, Monforte M, Hedberg-Oldfors C, Sabatelli M, Udd B, Boldrini R, Bertini E, Ricci E, Oldfors A
Journal of neurology 2016 Oct;263(10):2133-5
Journal of neurology 2016 Oct;263(10):2133-5
LC-MS/MS characterization of combined glycogenin-1 and glycogenin-2 enzymatic activities reveals their self-glucosylation preferences.
Nilsson J, Halim A, Larsson E, Moslemi AR, Oldfors A, Larson G, Nilsson J
Biochimica et biophysica acta 2014 Feb;1844(2):398-405
Biochimica et biophysica acta 2014 Feb;1844(2):398-405
A new muscle glycogen storage disease associated with glycogenin-1 deficiency.
Malfatti E, Nilsson J, Hedberg-Oldfors C, Hernandez-Lain A, Michel F, Dominguez-Gonzalez C, Viennet G, Akman HO, Kornblum C, Van den Bergh P, Romero NB, Engel AG, DiMauro S, Oldfors A
Annals of neurology 2014 Dec;76(6):891-8
Annals of neurology 2014 Dec;76(6):891-8
Dysregulation of multiple facets of glycogen metabolism in a murine model of Pompe disease.
Taylor KM, Meyers E, Phipps M, Kishnani PS, Cheng SH, Scheule RK, Moreland RJ
PloS one 2013;8(2):e56181
PloS one 2013;8(2):e56181
Molecular pathogenesis of a new glycogenosis caused by a glycogenin-1 mutation.
Nilsson J, Halim A, Moslemi AR, Pedersen A, Nilsson J, Larson G, Oldfors A
Biochimica et biophysica acta 2012 Apr;1822(4):493-9
Biochimica et biophysica acta 2012 Apr;1822(4):493-9
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Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- 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