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- 抗原 See all IDUA 抗体
- IDUA (Iduronidase, alpha-L- (IDUA))
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抗原表位
- AA 101-200
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适用
- 大鼠
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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, Western Blotting (WB)
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from 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 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 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
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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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
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Synonyms: IDA, MPS1, Alpha-L-iduronidase, IDUA
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). [provided by RefSeq, Jul 2008].
- 基因ID
- 3425
- UniProt
- P35475
- 途径
- Glycosaminoglycan Metabolic Process
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