AGA 抗体 (Middle Region)
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北京 101111
Quick Overview for AGA 抗体 (Middle Region) (ABIN2788660)
抗原
See all AGA 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- Middle Region
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原理
- AGA Antibody - middle region
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序列
- SMGFINEDLS TTASQALHSD WLARNCQPNY WRNVIPDPSK YCGPYKPPGI
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预测反应
- Cow: 86%, Dog: 79%, Guinea Pig: 85%, Horse: 79%, Human: 100%, Pig: 86%, Rat: 79%
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产品特性
- This is a rabbit polyclonal antibody against AGA. It was validated on Western Blot.
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纯化方法
- Affinity Purified
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anti-Aspartylglucosaminidase (AGA) antibody
AGA 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 28-245) antibodyAGA 适用: 人 WB, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 138-187) antibodyAGA 适用: 人, Cow, 犬, 豚鼠, 马, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 24-260) antibodyAGA 适用: 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 206-346) antibodyAGA 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 1-346) antibodyAGA 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- Optimal working dilution should be determined by the investigator.
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说明
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP61039-100UG
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.5 mg/mL
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缓冲液
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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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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注意事项
- prevent freeze-thaw cycles
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储存条件
- 4 °C,-20 °C
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储存方法
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- AGA (Aspartylglucosaminidase (AGA))
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别名
- AGA
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背景
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Background Information: Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme.
Gene Name: Aspartylglucosaminidase
Alternative Symbols: GA, AGU, ASRG
Protein Name: N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase
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分子量
- 36kDa
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基因ID
- 175
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NCBI登录号
- NP_001165459
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UniProt
- P20933
抗原
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