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Cat. No. ARG1543

PGPEP1 Knockout Raji Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Bone

  • Disease:

    Burkitt lymphoma

PGPEP1 Knockout Raji Polyclonal Cells, a CRISPR/Cas9-edited polyclonal knockout cell population derived from the EBV-positive Burkitt's lymphoma Raji B lymphoblast cell line. This tool enables targeted disruption of the PGPEP1 gene, which encodes a pyroglutamyl aminopeptidase involved in neuropeptide and peptide hormone processing. PGPEP1 regulates bioactive peptides such as TRH, neurotensin, and GnRH through interactions with prohormone convertases. This model is suited for neuropeptide processing studies, enzyme kinetics, and peptide hormone regulation assays using techniques like fluorogenic enzyme assays, western blotting, and mass spectrometry.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    Raji

    Cell Type

    B cell line

    Sex of Donor

    Male

    Age

    11 years

    Derived From Site

    In situ; Maxilla

    Gene Name

    PGPEP1

    Gene Identifier

    NCBI Gene ID 54858

    Morphology

    Lymphoblast-like

    Growth Mode

    Suspension

    Storage

    Liquid nitrogen (LN2)

  • Culture Conditions

    Growth medium

    RPMI 1640

    Supplement(s)

    10% Fetal Bovine Serum, 1% Penicillin-Streptomycin Solution

    Temperature

    37°C

    Atmosphere

    5% COâ‚‚

  • Quality Control

    Sterility testing

    The bacterial, yeast, and fungi are not detected in these cells by daily monitor.

    Mycoplasma testing

    Negative for mycoplasma through PCR analysis

  • Disclaimer

    Intended Use

    This product is intended for laboratory in vitro use only. It is not intended for diagnostic, therapeutic, or clinical applications.

    Disclaimer

    Ascent Research endeavors to provide accurate and up-to-date product information. However, no warranties or representations are made regarding its completeness or reliability. References to scientific literature and patents are for informational purposes only, and the customer assumes sole responsibility for verifying their accuracy.

    By accepting this product, the customer acknowledges and agrees to assume all risks associated with its receipt, handling, storage, disposal, and use, including compliance with all applicable safety and environmental regulations and precautions. Relevant laws, regulations, and ethical guidelines must be followed in conducting any research, modifications, or derivatives derived from this product.

    This product is provided "AS IS", and except as expressly stated herein, Ascent Research disclaims all other warranties, express or implied. Under no circumstances shall Ascent Research, its affiliates, or representatives be liable for indirect, incidental, consequential, or punitive damages arising from the use of this material. While Ascent Research employs rigorous quality control measures, we shall not be held responsible for damages resulting from misidentification or misinterpretation of the provided materials.

Description

PGPEP1 Knockout Raji Polyclonal Cells are a CRISPR/Cas9-edited polyclonal knockout cell population, providing a loss-of-function model for the PGPEP1 gene in the Homo sapiens Raji B lymphoblast cell line. The polyclonal population, generated via CRISPR/Cas9-mediated gene disruption, offers a heterogeneous knockout pool, facilitating studies of PGPEP1 function without clonal selection. This product is designed for researchers investigating neuropeptide processing and peptide hormone metabolism.

The Raji cell line is an EBV-positive Burkitt??s lymphoma-derived B lymphoblast, extensively used to model B cell biology and adaptive immune responses. Raji cells exhibit robust immunoglobulin production and are a well-established platform for examining signaling pathways intersecting with peptide hormone regulation. The integration of PGPEP1 knockout in this background enables exploration of how neuropeptide processing influences B cell function.

PGPEP1 encodes a pyroglutamyl aminopeptidase that catalyzes the removal of N-terminal pyroglutamyl residues from bioactive peptides, a critical step in maturation and inactivation. Key substrates include thyrotropin-releasing hormone (TRH), neurotensin, and gonadotropin-releasing hormone (GnRH). Enzymatic activity is influenced by upstream transcription factors such as SP1 and AP-1, and hormonal stimuli. PGPEP1 works in concert with prohormone convertases to generate mature peptides, which then activate cognate receptors and downstream signaling cascades. Disruption of PGPEP1 alters the repertoire of processed peptides, perturbing cellular signaling networks mediated by these neuropeptides.

In a B lymphoblast context, PGPEP1??s role in peptide processing may intersect with immune regulation. Whereas its primary characterized functions are in neuroendocrine tissues, the presence of neuropeptide receptors on immune cells suggests autocrine or paracrine modulation. This knockout model allows the dissection of PGPEP1-dependent peptide metabolism within an immune environment, potentially revealing implications for neuro-immune crosstalk and the modulation of adaptive immunity. Although no definitive disease association is established, alterations in PGPEP1 have been implicated in neurological disorders, and this cell model provides a simplified system to study its biochemistry.

The PGPEP1 Knockout Raji Polyclonal Cells are ideal for neuropeptide processing studies and enzyme kinetics characterization. Researchers can employ fluorogenic substrate assays to measure pyroglutamyl aminopeptidase activity directly, western blotting and RT-qPCR to assess gene and protein expression changes, immunofluorescence for subcellular localization, and mass spectrometry for global peptide profiling. This tool supports biomarker discovery efforts and high-throughput screening for modulators of peptide hormone pathways. For additional information, including availability and pricing, please contact Ascent Research.

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