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- 抗原 See all IDS 抗体
- IDS (Iduronate 2-Sulfatase (IDS))
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适用
- 人, 小鼠, 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 IDS antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human IDS (NP_006114.1).
- 亚型
- IgG
- Top Product
- Discover our top product IDS Primary Antibody
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anti-Iduronate 2-Sulfatase (IDS) (AA 95-289) antibody
IDS 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Iduronate 2-Sulfatase (IDS) antibodyIDS 适用: 人, 小鼠 WB, IHC, IHC (p), IF, FACS 宿主: 小鼠 Monoclonal 1D9 unconjugated
anti-Iduronate 2-Sulfatase (IDS) antibodyIDS 适用: 人, 小鼠, 大鼠, 犬, 猴 WB, IHC, IHC (p), IF, FACS 宿主: 小鼠 Monoclonal 4G2 unconjugated
anti-Iduronate 2-Sulfatase (IDS) (AA 34-290) antibodyIDS 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Iduronate 2-Sulfatase (IDS) (AA 1-550) antibodyIDS 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Iduronate 2-Sulfatase (IDS) (Internal Region) antibodyVerified IDS 适用: 人 WB, IHC, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Iduronate 2-Sulfatase (IDS) antibodyIDS 适用: 人, 小鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Iduronate 2-Sulfatase (IDS) (AA 38-137) antibodyIDS 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Iduronate 2-Sulfatase (IDS) (AA 1-312) antibodyIDS 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 3B4 unconjugated
anti-Iduronate 2-Sulfatase (IDS) (AA 1-550) antibodyIDS 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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- 应用备注
- WB 1:500-1:2000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 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
- IDS (Iduronate 2-Sulfatase (IDS))
- 别名
- IDS (IDS 产品)
- 背景
- This gene encodes a member of the sulfatase family of proteins. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. This enzyme is involved in the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed.
- 分子量
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Observed_MW: 76 kDa
Calculated_MW: 34 kDa/38 kDa/61 kDa
- 基因ID
- 3423
- UniProt
- P22304
- 途径
- Glycosaminoglycan Metabolic Process
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