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CHO/Human CDCP1 (NTF&CTF) Stable Cell Line

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Numéro de produit/spécification
Prix
Qté
CCHO-ATP235-2Vials (1Vial X 2)
$4785.00
ETA of in-stock products:2 business days
Total des articles Montant du produit$ 0

Détails du produit

    1. Genetically modified cell lines best reflect MOA (Mechanism of Action)
    2. Higher activity and larger assay window for robust and reproducible cell-based bioassay
    3. Comprehensive application data to support assay development and validation
    4. Full tracible record, stringent quality control and validated cell passage stability
    5. Parental cell line legally obtained from internationally recognized cell resource bank and commercially licensed
    6. Global commercial license assistance whenever regulatory filing is required
  • Description

    The CHO/Human CDCP1 (NTF&CTF) Stable Cell Line was engineered to express the cleaved human CDCP1 by co-expressing the N-terminal fragment (NTF) and the C-terminal fragment (CTF) of human CDCP1 (Uniprot: Q9H5V8-1). Surface expression of human CDCP1 (NTF&CTF) was confirmed by flow cytometry.

  • Application

    • Useful for cell-based CDCP1 (NTF&CTF) binding assay

  • Growth Properties

    Adherent

  • Selection Marker

    Puromycin (2 μg/mL) + Hygromycin B (20 μg/mL)

  • Complete Growth Medium

    F-12K + 10% FBS

  • Freeze Medium

    Serum-free cell cryopreservation medium

  • Quantity

    1 vial contains at least 5×10^6 cells in 1 mL serum-free cryopreservation medium

  • Storage

    Frozen in liquid nitrogen.

  • Mycoplasma Testing

    Negative

  • Sterility Testing

    Negative

  • Instructions for Use

    See data sheet for detailed culturing and assay protocol.

  • ACRO Quality Management System

    1. QMS(ISO, GMP)
    2. Quality Advantages
    3. Quality Control Process

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Affichage des données

  • Receptor Assay

     CDCP1 FACS

    Expression analysis of human CDCP1 (NTF&CTF) on CHO/Human CDCP1 (NTF&CTF) Stable Cell Line by FACS.
    Cell surface staining was performed on CHO/Human CDCP1 (NTF&CTF) Stable Cell Line or negative control cell using PE-labeled anti-human CDCP1 antibody.

    Protocol
  •  CDCP1 FACS

    Expression analysis of human CDCP1 (NTF&CTF) on CHO/Human CDCP1 (NTF&CTF) Stable Cell Line by FACS.
    Cell surface staining was performed on CHO/Human CDCP1 (NTF&CTF) Stable Cell Line or negative control cell using the antibody specifically recognizing an epitope on the N-terminal fragment (NTF) of human CDCP1, followed by staining with PE anti-human IgG Fc antibody.

    Protocol
  •  CDCP1 FACS

    Expression analysis of human CDCP1 (NTF&CTF) on CHO/Human CDCP1 (NTF&CTF) Stable Cell Line by FACS.
    Cell surface staining was performed on CHO/Human CDCP1 (NTF&CTF) Stable Cell Line or negative control cell using the antibody specifically recognizing an epitope on the C-terminal fragment (CTF) of human CDCP1, followed by staining with PE anti-human IgG Fc antibody.

    Protocol
  •  CDCP1 FACS

    Expression analysis of human CDCP1 (NTF&CTF) on CHO/Human CDCP1 (NTF&CTF) Stable Cell Line by FACS.
    Cell surface staining was performed on CHO/Human CDCP1 (NTF&CTF) Stable Cell Line or negative control cell using the antibody specifically targeting the cleaved human CDCP1 (NTF&CTF), followed by staining with PE anti-human IgG Fc antibody.

    Protocol
*Please contact us if you are interested in related cell pool service.

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  • Limited Use&License Disclosure

    BY USE OF THIS PRODUCT, RESEARCHER AGREES TO BE BOUND BY THE FOLLOWING TERMS OF LIMITED USE OF THIS CELL LINE PRODUCT.

    1. If the researcher is not willing to accept the terms of limited use of this cell line product, and the product is unused, ACRO will accept return of the unused product.
    2. Researchers may use this product for research use only, no commercial use is allowed. "Commercial use" means any and all uses of this product and derivatives by a party for profit or other consideration and may include but is not limited to use in: (1) product manufacture; and (2) to provide a service, information or data; and/or resale of the product or its derivatives, whether or not such product or derivatives are resold for use in research.
    3. This cell line is neither intended for any animal or human therapeutic purposes nor for any direct human in vivo use. You have no right to share, modify, transfer, distribute, sell, sublicense, or otherwise make the cell line available for use to other researchers, laboratories, research institutions, hospitals, universities, or service organizations.
    4. ACROBIOSYSTEMS MAKES NO WARRANTIES OR REPRESENTATIONS OF ANY KIND, EITHER EXPRESSED OR IMPLIED, WITH RESPECT TO THE SUITABILITY OF THE CELL LINE FOR ANY PARTICULAR USE.
    5. ACROBIOSYSTEMS ACCEPTS NO LIABILITY IN CONNECTION WITH THE HANDLING OR USE OF THE CELL LINE.
    6. Modifications of the cell line, transfer to a third party, or commercial use of the cell line may require a separate license and additional fees. Please contact order@acrobiosystems.com for further details.

Progrès de frontière

 
Progrès du développement médicamenteux
  • Nom anglais:

    CUB domain-containing protein 1

  • Catégorie:

  • Nombre de médicaments répertoriés:

    0 Détails

  • Nombre de médicaments cliniques:

    0 Détails

  • Étape de développement la plus élevée:

    Preclinical

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