IDS 抗体 (AA 1-300)
Quick Overview for IDS 抗体 (AA 1-300) (ABIN7115175)
抗原
See all IDS 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 1-300
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原理
- IDS antibody
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纯化方法
- Protein A+G purification
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纯度
- ≥95 % as determined by SDS-PAGE
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免疫原
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Immunogen sequence: 1-300aa
Immunogen: iduronate 2-sulfatase
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亚型
- IgG1
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anti-Iduronate 2-Sulfatase (IDS) (AA 95-289) antibody
IDS 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Iduronate 2-Sulfatase (IDS) antibodyIDS 适用: 人, 小鼠, 大鼠, 犬, 猴 WB, IHC, IF, IHC (p), FACS 宿主: 小鼠 Monoclonal 4G2 unconjugated
anti-Iduronate 2-Sulfatase (IDS) antibodyIDS 适用: 人, 小鼠 WB, IHC, IF, IHC (p), FACS 宿主: 小鼠 Monoclonal 1D9 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) (Internal Region) antibodyVerified IDS 适用: 人 WB, IHC, ELISA 宿主: 山羊 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) 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 154-203) antibodyIDS 适用: 人, 犬, 猴, Cow, 豚鼠, 兔 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Iduronate 2-Sulfatase (IDS) (AA 1-312) antibodyIDS 适用: 人 WB, IHC, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 3B4 unconjugated
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应用备注
- WB: 1:500-1:1000, IHC: 1:20-1:200, IF: 1:20-1:200
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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
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,
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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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注意事项
- Avoid repeated freeze / thaw cycles.
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储存条件
- -20 °C
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储存方法
- -20°C for 12 months
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有效期
- 12 months
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- IDS (Iduronate 2-Sulfatase (IDS))
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别名
- IDS
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背景
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Synonyms: Iduronate 2-sulfatase|Alpha-L-iduronate sulfate sulfatase (Idursulfase)|Iduronate 2-sulfatase 42 kDa chain|Iduronate 2-sulfatase 14 kDa chain|IDS|SIDS
Background: Iduronate 2-sulfatase (IDS) is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations causing IDS deficiency in humans result in the lysosomal storage of these glycosaminoglycans and Hunter syndrome, an X chromosome-linked disease. IDS is synthesized as two precursor forms of 76 and 90 kDa that are converted, through a 62 kDa intermediate, to 55 and 45 kDa mature polypeptides due to an internal proteolytic cleavage (PMID: 10838181).
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分子量
- 76 kDa, 55 kDa
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基因ID
- 3423
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UniProt
- P22304
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途径
- Glycosaminoglycan Metabolic Process
抗原
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