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Kyphoscoliosis Peptidase 抗体 (AA 51-150)

This anti-Kyphoscoliosis Peptidase antibody is a 兔 多克隆 antibody detecting Kyphoscoliosis Peptidase in WB, ELISA, IHC (fro), IF (cc), IF (p), IHC (p) 和 ICC. Suitable for 人.
产品编号 ABIN1386443
发货至: 中国
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中国
北京 101111
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Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Kyphoscoliosis Peptidase 抗体 (AA 51-150) (ABIN1386443)

抗原

See all Kyphoscoliosis Peptidase (KY) 抗体
Kyphoscoliosis Peptidase (KY)

适用

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宿主

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克隆类型

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多克隆

标记

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This Kyphoscoliosis Peptidase antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
  • 抗原表位

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    AA 51-150

    预测反应

    Human,Mouse,Rat,Dog,Pig

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human Kyphoscoliosis peptidase

    亚型

    IgG
  • 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

    Kyphoscoliosis Peptidase (KY)

    别名

    KY/Kyphoscoliosis peptidase

    背景

    Synonyms: KY, KY_HUMAN, Kyphoscoliosis peptidase.

    Background: KY peptidase (Kyphoscoliosis peptidase) is a 561 amino acid cytoskeleton protease that interacts with several sarcomeric cytoskeletal proteins, including Filamin 2. KY peptidase probably plays a role in the maturation, function and stabilization of the neuromuscular junction. KY-null mouse mutants exhibit distinct irregular subceullular Filamin 2 localization, suggesting that KY peptidase deficiency may be the cause of several types of limb-girdle muscular dystrophies.

    基因ID

    339855

    途径

    Skeletal Muscle Fiber Development
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