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- 抗原 See all IDUA 抗体
- IDUA (Iduronidase, alpha-L- (IDUA))
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适用
- 人, 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This IDUA antibody is un-conjugated
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应用范围
- ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Antigen affinity purification
- 免疫原
- Synthetic peptide of human IDUA
- 亚型
- IgG
- Top Product
- Discover our top product IDUA Primary Antibody
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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 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Iduronidase, alpha-L- (IDUA) (AA 101-200) antibodyIDUA 适用: 大鼠 WB, ELISA 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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- 应用备注
- IHC 1:30-1:150, ELISA 1:5000-1:10000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.96 mg/mL
- 缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- IDUA (Iduronidase, alpha-L- (IDUA))
- 别名
- IDUA (IDUA 产品)
- 别名
- IDA antibody, MPS1 antibody, 6030426D08 antibody, alpha-L-iduronidase antibody, MGC80842 antibody, si:ch211-12e13.9 antibody, IDUA antibody, iduronidase, alpha-L- antibody, iduronidase, alpha-L- L homeolog antibody, alpha-L-iduronidase antibody, IDUA antibody, Idua antibody, idua.L antibody, idua antibody, LOC5564727 antibody
- 背景
- 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).
- UniProt
- P35475
- 途径
- Glycosaminoglycan Metabolic Process
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