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Western blotAntibody data
- Antibody Data
- Antigen structure
- References [4]
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- Product number
- ABIN356948 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Phosphorylase, Glycogen, Muscle (PYGM) (C-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the C-terminal region of human PYGM.
- Description
- Protein A column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- C-Term
- Vial size
- 0.4 mL
- Concentration
- 0.25 mg/mL
- Storage
- Store the antibody at 2 - 8°C up to one month or (in aliquots) at -20°C for longer.
- Handling
- Avoid repeated freezing and thawing.
Submitted references cDNA microarray analysis of gene expression profiles in human placenta: up-regulation of the transcript encoding muscle subunit of glycogen phosphorylase in preeclampsia.
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families.
Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease.
A novel nonsense mutation (R269X) in the myophosphorylase gene in a patient with McArdle disease.
Tsoi SC, Cale JM, Bird IM, Kay HH
Journal of the Society for Gynecologic Investigation 2003 Dec;10(8):496-502
Journal of the Society for Gynecologic Investigation 2003 Dec;10(8):496-502
Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families.
Hadjigeorgiou GM, Sadeh M, Musumeci O, Dabby R, De Girolami L, Naini A, Papadimitriou A, Shanske S, DiMauro S
Neuromuscular disorders : NMD 2002 Nov;12(9):824-7
Neuromuscular disorders : NMD 2002 Nov;12(9):824-7
Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease.
Bruno C, Lanzillo R, Biedi C, Iadicicco L, Minetti C, Santoro L
Neuromuscular disorders : NMD 2002 Jun;12(5):498-500
Neuromuscular disorders : NMD 2002 Jun;12(5):498-500
A novel nonsense mutation (R269X) in the myophosphorylase gene in a patient with McArdle disease.
Deschauer M, Opalka JR, Lindner A, Zierz S
Molecular genetics and metabolism 2001 Dec;74(4):489-91
Molecular genetics and metabolism 2001 Dec;74(4):489-91
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