Antibody data
- Antibody Data
- Antigen structure
- References [5]
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- Validations
- Western blot [3]
- ELISA [1]
- Immunohistochemistry [1]
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- Product number
- ABIN396266 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Galactose-1-Phosphate Uridylyltransferase (GALT) (AA 1-380) antibody
- Antibody type
- Monoclonal
- Description
- This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
- Reactivity
- Human
- Host
- Mouse
- Epitope
- AA 1-380
- Isotype
- IgG
- Antibody clone number
- 4C11
- Vial size
- 100 μg
- Storage
- Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Submitted references Molecular and biochemical characterization of the GALT gene in Korean patients with galactose-1-phosphate uridyltransferase deficiency.
Analysis of galactosemia-linked mutations of GALT enzyme using a computational biology approach.
Classical galactosemia in Estonia: selective neonatal screening, incidence, and genotype/phenotype data of diagnosed patients.
New genetic associations detected in a host response study to hepatitis B vaccine.
Galactose-1-phosphate uridyl transferase deficiency is not associated with Müllerian aplasia in Dutch patients.
Ko DH, Chang HE, Song SH, Park KU, Kim JQ, Kim MC, Song YH, Hong YH, Lee DH, Song J
Clinica chimica acta; international journal of clinical chemistry 2010 Oct 9;411(19-20):1506-10
Clinica chimica acta; international journal of clinical chemistry 2010 Oct 9;411(19-20):1506-10
Analysis of galactosemia-linked mutations of GALT enzyme using a computational biology approach.
Facchiano A, Marabotti A
Protein engineering, design & selection : PEDS 2010 Feb;23(2):103-13
Protein engineering, design & selection : PEDS 2010 Feb;23(2):103-13
Classical galactosemia in Estonia: selective neonatal screening, incidence, and genotype/phenotype data of diagnosed patients.
Ounap K, Joost K, Temberg T, Krabbi K, Tõnisson N
Journal of inherited metabolic disease 2010 Apr;33(2):175-6
Journal of inherited metabolic disease 2010 Apr;33(2):175-6
New genetic associations detected in a host response study to hepatitis B vaccine.
Davila S, Froeling FE, Tan A, Bonnard C, Boland GJ, Snippe H, Hibberd ML, Seielstad M
Genes and immunity 2010 Apr;11(3):232-8
Genes and immunity 2010 Apr;11(3):232-8
Galactose-1-phosphate uridyl transferase deficiency is not associated with Müllerian aplasia in Dutch patients.
Nijland R, Hartog FE, Wevers RA, Wanders RJ, Willemsen WN
Journal of pediatric and adolescent gynecology 2009 Aug;22(4):229-31
Journal of pediatric and adolescent gynecology 2009 Aug;22(4):229-31
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Supportive validation
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- IHC