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Cathepsin K 抗体

CTSK 适用: 人, 大鼠, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN732038
发货至: 中国
  • 抗原 See all Cathepsin K (CTSK) 抗体
    Cathepsin K (CTSK)
    适用
    • 59
    • 33
    • 26
    • 9
    • 7
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 大鼠, 小鼠
    宿主
    • 62
    • 23
    • 1
    克隆类型
    • 64
    • 22
    多克隆
    标记
    • 45
    • 11
    • 10
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    This Cathepsin K antibody is un-conjugated
    应用范围
    • 64
    • 32
    • 23
    • 15
    • 11
    • 11
    • 8
    • 8
    • 5
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB)
    交叉反应
    小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human Capsin K
    亚型
    IgG
    Top Product
    Discover our top product CTSK Primary Antibody
  • 应用备注
    WB: 1:100-1000, IHC-P: 1:100-500, IF(IHC-P): 1:50-200
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
    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
    Store at -20°C for 12 months.
    有效期
    12 months
  • 抗原
    Cathepsin K (CTSK)
    别名
    Cathepsin K (CTSK 产品)
    背景

    Synonyms: Cathepsin K, Procathepsin K, Cathepsin K precursor, Cathepsin O, Cathepsin O1, Cathepsin O2, Cathepsin X, CathepsinK, CTS02, CTSK, CTSK protein, CTSO, CTSO1, CTSO2, MGC23107, PKND, PYCD, Pycnodysostosis, cath-K, CK.

    Background: The protein encoded by this gene is a lysosomal cysteine proteinase involved in bone remodeling and resorption. This protein, which is a member of the peptidase C1 protein family, is predominantly expressed in osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers, where it could contribute to tumor invasiveness. Mutations in this gene are the cause of pycnodysostosis, an autosomal recessive disease characterized by osteosclerosis and short stature. This gene may be subject to RNA editing. [provided by RefSeq, Jul 2008].

    基因ID
    1513
    途径
    Activation of Innate immune Response, Toll-Like Receptors Cascades
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