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GALNS 抗体 (AA 1-100) (AbBy Fluor® 594)

This anti-GALNS antibody is a 兔 多克隆 antibody detecting GALNS in WB, IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN2813540
发货至: 中国

Quick Overview for GALNS 抗体 (AA 1-100) (AbBy Fluor® 594) (ABIN2813540)

抗原

See all GALNS 抗体
GALNS (Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))

适用

  • 48
  • 14
  • 13

宿主

  • 52
  • 2
  • 1

克隆类型

  • 55
多克隆

标记

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  • 1
  • 1
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This GALNS antibody is conjugated to AbBy Fluor® 594

应用范围

  • 41
  • 20
  • 17
  • 13
  • 12
  • 12
  • 12
  • 9
  • 8
  • 6
  • 3
  • 1
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    • 5
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    • 3
    • 3
    • 2
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    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 1-100

    预测反应

    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human GALNS

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    GALNS (Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))

    别名

    GALNS

    背景

    Synonyms: Chondroitinase, Chondroitinsulfatase, FLJ00319, FLJ17434, FLJ42844, FLJ98217, Galactosamine N acetyl 6 sulfate sulfatase, Galactose 6 sulfate sulfatase, GALNAC6S, GalNAc6S sulfatase, GAS, mFLJ00319, MPS4A, N acetylgalactosamine 6 sulfatase, N acetylgalactosamine 6 sulfate sulfatase, GALNS_HUMAN.

    Background: Chondroitinase is a 522 amino acid protein that localizes to the lysosome and functions as an exohydrolase that is essential for the degradation of glycosaminoglycans, keratan sulfate and chondroitin 6-sulfate. Using calcium as a cofactor, Chondroitinase, which exists as a disulfide linked oligomer, catalyzes the hydrolysis of the 6-sulfate group on target substrates. Defects in the gene encoding Chondroitinase are the cause of mucopolysaccharidosis type 4A (MPS4A), an autosomal recessive lysosomal storage disease that is characterized by the intracellular accumulation of keratan sulfate and chondroitin-6-sulfate and is associated with dental anomalies, short stature and, in some cases, death in the second or third decade of life.

    基因ID

    2588

    途径

    Glycosaminoglycan Metabolic Process
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