AGL 抗体
Quick Overview for AGL 抗体 (ABIN7001167)
抗原
See all AGL 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Synthetic peptide of human AGL
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亚型
- IgG
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anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) (AA 1479-1510), (C-Term) antibody
AGL 适用: 人 WB, IF 宿主: 兔 Polyclonal RB4978 unconjugated
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) (AA 357-387) antibodyAGL 适用: 人 WB, IF 宿主: 兔 Polyclonal RB4976 unconjugated
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) (N-Term) antibodyAGL 适用: 人 WB, IF 宿主: 兔 Polyclonal RB5106 unconjugated
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) (AA 1-1532) antibodyAGL 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) (AA 1217-1378) antibodyAGL 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) (AA 1233-1532) antibodyAGL 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) antibodyAGL 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) antibodyKD Validated AGL 适用: 人, 小鼠, 大鼠 WB, IF, IHC, ICC, FACS 宿主: 兔 Monoclonal unconjugated Recombinant Antibody
anti-Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL) (AA 1487-1516), (C-Term) antibodyAGL 适用: 人 WB, IF, EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
- IHC 1:25-1:100
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.2 mg/mL
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缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- AGL (Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
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别名
- AGL
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背景
- This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described.
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NCBI登录号
- NP_000019
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UniProt
- P35573
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途径
- Cellular Glucan Metabolic Process
抗原
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