IDUA 抗体 (Middle Region)
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北京 101111
Quick Overview for IDUA 抗体 (Middle Region) (ABIN2789574)
抗原
See all IDUA 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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序列
- MENQLLPGFE LMGSPSGYFT DFDDKQQVFE WKDLVSLLAR RYIGRYGLTH
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预测反应
- Cow: 86%, Dog: 90%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 86%, Rat: 93%
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产品特性
- This is a rabbit polyclonal antibody against Idua. It was validated on Western Blot.
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纯化方法
- Affinity Purified
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免疫原
- The immunogen is a synthetic peptide directed towards the middle region of mouse IDUA
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anti-Iduronidase, alpha-L- (IDUA) (AA 236-264) antibody
IDUA 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB26860 unconjugated
anti-Iduronidase, alpha-L- (IDUA) (AA 28-306) antibodyIDUA 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Iduronidase, alpha-L- (IDUA) (AA 28-653) antibodyIDUA 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Iduronidase, alpha-L- (IDUA) antibodyIDUA 适用: 人, 小鼠 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-Iduronidase, alpha-L- (IDUA) antibodyIDUA 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Iduronidase, alpha-L- (IDUA) (AA 101-200) antibodyIDUA 适用: 大鼠 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-Iduronidase, alpha-L- (IDUA) (AA 121-170) antibodyIDUA 适用: 人, 小鼠, 豚鼠, 马, Cow, Hamster WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- Liquid. 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
- Avoid repeat freeze-thaw cycles.
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储存条件
- -20 °C
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储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- IDUA (Iduronidase, alpha-L- (IDUA))
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别名
- Idua
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背景
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This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I).
Alias Symbols: IDA, MPS1
Protein Size: 281 -
分子量
- 30 kDa
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基因ID
- 3425
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NCBI登录号
- NM_000203, NP_000194
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UniProt
- P35475
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途径
- Glycosaminoglycan Metabolic Process
抗原
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