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Cleaved-Cathepsin D HC (L169) Polyclonal Antibody
Cleaved-Cathepsin D HC (L169) Polyclonal Antibody
  • 商品货号:FAB2600030
  • WB IHC IF ELISA ICC IP FC
    活动价: ¥680元
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    • 靶点-Target: Cathepsin D
    • MW(Observed): 27kD
    • 宿主物种-Host Species: Rabbit
    • 同种型-Isotype: IgG
    • 修饰-Modification: Unmodified
    • 推荐稀释比: WB 1:500-1:2000;ELISA 1:40000;Not yet tested in other applications.
    • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
    • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
    • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
    • 浓度: 1 mg/ml
    • 克隆性: Polyclonal
    • 免疫原: The antiserum was produced against synthesized peptide derived from human CATD. AA range:150-199
    • 特异性: Cleaved-Cathepsin D HC (L169) Polyclonal Antibody detects endogenous levels of fragment of activated Cathepsin D HC protein resulting from cleavage adjacent to L169.
    • 基因名称: CTSD
    • 蛋白名称: Cathepsin D
    • Organism-1: Human
    • 基因ID-1: 1509
    • SwissProt-1: P07339
    • Organism-2: Mouse
    • SwissProt-2: P18242
    • 背景: This gene encodes a member of the A1 family of peptidases. The encoded preproprotein is proteolytically processed to generate multiple protein products. These products include the cathepsin D light and heavy chains, which heterodimerize to form the mature enzyme. This enzyme exhibits pepsin-like activity and plays a role in protein turnover and in the proteolytic activation of hormones and growth factors. Mutations in this gene play a causal role in neuronal ceroid lipofuscinosis-10 and may be involved in the pathogenesis of several other diseases, including breast cancer and possibly Alzheimer's disease. [provided by RefSeq, Nov 2015],
    • 细胞定位: Lysosome. Melanosome. Secreted, extracellular space. Identified by mass spectrometry in melanosome fractions from stage I to stage IV. In aortic samples, detected as an extracellular protein loosely bound to the matrix (PubMed:20551380). .
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