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IDS 抗体

This anti-IDS antibody is a 兔 多克隆 antibody detecting IDS in WB 和 ELISA. Suitable for 人.
产品编号 ABIN7229018
发货至: 中国

Quick Overview for IDS 抗体 (ABIN7229018)

抗原

See all IDS 抗体
IDS (Iduronate 2-Sulfatase (IDS))

适用

  • 42
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宿主

  • 33
  • 10
  • 3

克隆类型

  • 39
  • 7
多克隆

标记

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  • 1
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  • 1
  • 1
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  • 1
  • 1
  • 1
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This IDS antibody is un-conjugated

应用范围

  • 44
  • 17
  • 13
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  • 8
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  • 3
Western Blotting (WB), ELISA
  • 原理

    IDS Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of IDS protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human IDS protein

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    IDS (Iduronate 2-Sulfatase (IDS))

    别名

    IDS

    背景

    Rabbit Anti-IDS Polyclonal Antibody,Iduronate 2-sulfatase, Alpha-L-iduronate sulfate sulfatase, Idursulfase,IDS encodes a member of the sulfatase family of proteins. Iduronate 2-Sulfatase 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.,IDS

    分子量

    observerd band 60kDa

    基因ID

    3423

    UniProt

    P22304

    途径

    Glycosaminoglycan Metabolic Process
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