IDUA 抗体 (AA 1-87) (Biotin)
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北京 101111
Quick Overview for IDUA 抗体 (AA 1-87) (Biotin) (ABIN7999060)
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
- AA 1-87
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原理
- Anti-IDUA Antibody Biotin Conjugated
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交叉反应 （详细）
- No cross reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human INSIG1 recombinant protein (Position: M1-R87).
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亚型
- IgG
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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) antibodyIDUA 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal 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) (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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应用备注
- Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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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
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.
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有效期
- 12 months
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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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Background: 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).
Gene Full Name: alpha-L-iduronidase
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基因ID
- 3425
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UniProt
- P35475
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途径
- Glycosaminoglycan Metabolic Process
抗原
-
