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IDUA 抗体 (AA 101-200)

IDUA 适用: 大鼠 ELISA, WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1713845
发货至: 中国
  • 抗原 See all IDUA 抗体
    IDUA (Iduronidase, alpha-L- (IDUA))
    抗原表位
    • 8
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 101-200
    适用
    • 33
    • 13
    • 4
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    大鼠
    宿主
    • 29
    • 2
    • 2
    克隆类型
    • 31
    • 2
    多克隆
    标记
    • 16
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This IDUA antibody is un-conjugated
    应用范围
    • 21
    • 15
    • 12
    • 8
    • 3
    • 2
    • 1
    • 1
    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
  • 应用备注
    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
  • 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
  • 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

    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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