Antibody data
- Antibody Data
- Antigen structure
- References [2]
- Comments [0]
- Validations
- Western blot [2]
- Immunohistochemistry [2]
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- Product number
- ABIN2845755 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-Glucosidase, Alpha, Acid (GAA) (AA 174-203), (N-Term) antibody
- Antibody type
- Polyclonal
- Description
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Reactivity
- Human
- Host
- Rabbit
- Epitope
- AA 174-203, N-Term
- Antibody clone number
- RB18979
- Vial size
- 80 μL
- Storage
- GAA Antibody (N-term) can be refrigerated at 2-8°C for up to 6 months. For long term storage, place the at -20°C.
Submitted references Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.
Silent exonic mutation in the acid-alpha-glycosidase gene that causes glycogen storage disease type II by affecting mRNA splicing.
Aoyama Y, Ozer I, Demirkol M, Ebara T, Murase T, Podskarbi T, Shin YS, Gokcay G, Okubo M
Journal of human genetics 2009 Nov;54(11):681-6
Journal of human genetics 2009 Nov;54(11):681-6
Silent exonic mutation in the acid-alpha-glycosidase gene that causes glycogen storage disease type II by affecting mRNA splicing.
Maimaiti M, Takahashi S, Okajima K, Suzuki N, Ohinata J, Araki A, Tanaka H, Mukai T, Fujieda K
Journal of human genetics 2009 Aug;54(8):493-6
Journal of human genetics 2009 Aug;54(8):493-6
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- WB
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- WB
Supportive validation
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- antibodies-online (provider)
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- Experimental details
- IHC
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- IHC