Merck Millipore代理06-114 Anti-Cathepsin D Antibody;store at +2℃ to +8℃

2025-06-28

货号:06-114

品牌:Merck Millipore

规格:100Ug

目录价:¥5666.00

市场价格:¥4816.10

会员价格:¥4532.80

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Anti-Cathepsin D Antibody | 06-114 View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Specificity: This antibody recognizes Cathepsin D. View All» Molecular Weight: Observed molecular weight at ~58 kDa. Protein is glycosylated and may run slightly higher than predicted. Predicted molecular weight of the active form is ~46 kDa and ~ 54 kDa for the precursor form. View All» Epitope: Heavy Chain View All» Immunogen: GST-tagged recombinant protein corresponding to human Cathepsin D at the heavy chain. View All» Background Information: Cathepsin D is synthesized as a 54kDa precursor which is proteolytically processed to an intermediate 48kDa single chain which matures into more stable 34kDa and 14kDa two chain form. It is an estrogen-regulated lysosomal protease that has been suggested to facilitate cancer cell migration and invasion by digesting the basement membrane, extracellular matrix, and connective tissue. Because of its mitogenic and proteolytic activities, it has been implicated as a prognostic marker in many tumor types, especially breast cancer. Cathepsin D is expressed in epithelial cells as well as in macrophages. Immunoreactivity of cancer cells and tissue infiltrating macrophages must be recorded separately. View All» Species Reactivity: Human View All» Species Reactivity Note: Proven to react with human. 84% sequence homology to mouse and rat. View All» Application Notes: Immunocytochemistry Analysis: 1:500 dilution from a previous lot detected Cathepsin D in A431 and HeLa cell lystes. View All» Control: A431 cell lysate View All» Quality Assurance: Evaluated by Western Blot in A431 cell lysate.Western Blot Analysis: 1 µg/mL of this antibody detected Cathepsin D on 10 µg of A431 cell lysate. View All» Purification Method: Affinity Purfied View All» Presentation: Purified rabbit polyclonal in buffer containing 0.1 M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.05% sodium azide. View All» Storage Conditions: Stable for 1 year at 2-8°C from date of receipt. View All» UniProt Number: P07339 View All» Entrez Gene Number: NP_001900 View All» Gene Symbol:

  • CTSD

  • CLN10

  • CPSD

    View All» Alternate Names:
    • cathepsin D

    • cathepsin D (lysosomal aspartyl protease)

    • lysosomal aspartyl peptidase

    • lysosomal aspartyl protease

      View All» Usage Statement: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. View All» Key Applications:
      • Western Blotting

      • Immunocytochemistry

        View All» Entrez Gene Summary: This gene encodes a lysosomal aspartyl protease composed of a dimer of disulfide-linked heavy and light chains, both produced from a single protein precursor. This proteinase, which is a member of the peptidase C1 family, has a specificity similar to but narrower than that of pepsin A. Transcription of this gene is initiated from several sites, including one which is a start site for an estrogen-regulated transcript. Mutations in this gene are involved in the pathogenesis of several diseases, including breast cancer and possibly Alzheimer disease. View All» UniProt Summary: FUNCTION: Acid protease active in intracellular protein breakdown. Involved in the pathogenesis of several diseases such as breast cancer and possibly Alzheimer disease.SIZE: 412 amino acids; 44552 Da SUBUNIT: Consists of a light chain and a heavy chain.SUBCELLULAR LOCATION: Lysosome. Melanosome. Note=Identified by mass spectrometry in melanosome fractions from stage I to stage IV.DISEASE: Defects in CTSD are the cause of neuronal ceroid lipofuscinosis 10 (CLN10) [MIM:610127]; also known as neuronal ceroid lipofuscinosis due to cathepsin D deficiency. The neuronal ceroid lipofuscinosis are a group of progressive neurodegenerative diseases in children and in adults, characterized by visual and mental decline, motor disturbance, epilepsy and behavioral changes.SIMILARITY: Belongs to the peptidase A1 family. View All» Product Name: Anti-Cathepsin D View All» Concentration: 1.0 mg/mL View All» Antibody Type: Polyclonal Antibody View All» Qty/Pk: 100 μg View All» Format: Affinity Purified View All» Host: Rabbit View All»

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