IDUA Protein (Myc-DYKDDDDK Tag)
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- 抗原 See all IDUA 蛋白
- IDUA (Iduronidase, alpha-L- (IDUA))
- 蛋白类型
- Recombinant
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宿主
- 人
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资源
- HEK-293 Cells
- 标记
- This IDUA protein is labelled with Myc-DYKDDDDK Tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human Alpha-L-iduronidase / IDUA protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product IDUA 蛋白
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Iduronidase, alpha-L- (IDUA) (AA 17-634) protein (His tag)
Crystallography grade IDUA 宿主: 小鼠 宿主: Insect Cells Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. SDS, WB, ELISA, Crys
Iduronidase, alpha-L- (IDUA) (AA 28-653) protein (His tag)IDUA 宿主: 人 宿主: 大肠杆菌（E. Coli） Recombinant > 90 % SDS
Iduronidase, alpha-L- (IDUA) (AA 28-653) protein (His tag)IDUA 宿主: 人 宿主: 酵母菌 Recombinant > 90 % SDS
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- 应用备注
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - 说明
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The tag is located at the C-terminal.
- 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- 储存条件
- -80 °C
- 储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- 抗原
- IDUA (Iduronidase, alpha-L- (IDUA))
- 别名
- Iduronidase, alpha-L (Idua) (IDUA 产品)
- 别名
- IDA Protein, MPS1 Protein, 6030426D08 Protein, alpha-L-iduronidase Protein, MGC80842 Protein, si:ch211-12e13.9 Protein, IDUA Protein, iduronidase, alpha-L- Protein, iduronidase, alpha-L- L homeolog Protein, alpha-L-iduronidase Protein, IDUA Protein, Idua Protein, idua.L Protein, idua Protein, LOC5564727 Protein
- 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).
- 分子量
- 70 kDa
- NCBI登录号
- NP_000194
- 途径
- Glycosaminoglycan Metabolic Process
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