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DKK1 (dickkopf-related protein 1) is a member of the dickkopf family. This secreted protein family shares a similar conserved cysteine domain and inhibits the Wnt/β-catenin pathway by causing proteasome β-catenin degradation, inducing apoptosis and preventing cell proliferation. DKK1 is a discovered secretory glycoprotein that induces the head formation and is an endogenous inhibitor of the canonical Wnt/β-catenin signaling pathway. It has been found to be involved in many pathophysiological processes in the body. Abnormal expression of DKK1 not only alters the expression of related proteins and genes in the canonical Wnt/β-catenin signaling pathway but also alters the expression of related proteins and genes in other signaling pathways.
Figure 1: DKK1 regulation of signaling pathways (Michael H Kagey. 2017).
Numerous studies have shown that it plays an important role in embryonic development, nerve regeneration, and synapse formation. Therefore, its role in neuropsychiatric disorders, such as neurodevelopmental disorders, cognitive disorders, and mood disorders, has attracted increasing attention. At present, the role of DKK1 in Alzheimer's disease (AD) is one of the research hotspots.
Elevated levels of DKK1 in plasma and peripheral blood in patients with multiple myeloma are associated with osteolytic lesions. Due to the role of DKK1 in inflammation-induced bone loss, DKK1 is currently being studied as a target for medical and dental treatment strategies.
In addition, recent studies have shown that DKK1 may be an ideal target for cancer immunotherapy. Interestingly, the DKK1-CKAP4-PI3K/AKT signaling pathway also plays a role in the proliferation of pancreatic cancer cells. It may be useful to further study the mechanism of DKK1 and use it alone as a biomarker or in combination with other biomarkers.
DKK1 Gene Editing Service
CRISPR/Cas9 PlatformCB, a global leading biotechnological company specializing in gene editing, is dedicated to offering comprehensive CRISPR/Cas9 gene editing services and products to a wide range of genomics researchers. Based on our platform, we can help you effectively control target genes deleted, inserted or point mutated in cells or animals via CRISPR/Cas9 technology.
With deep gene editing knowledge and extensive experience in experimental operation and data processing, we have successfully implemented DKK1 CRISPR/Cas9 gene edited in both easy-to-transfect cell lines and hard-to-transfect cells. To support your projects, we will offer you full-length custom DKK1 gene editing service from strategy design to final stable cells. Our DKK1 gene editing cell line generation services include:
➢ gRNA design and synthesis
➢ Transfect the cell lines you're interested
➢ Select the high expression cells and sort monoclonal cell
➢ Validate the knockout/knockin/point mutation of DKK1 by PCR and sequencing
➢ Produce cryogenic preserved vials of stable cells and a final report
Typically, we develop CRISPR-mediated gene editing cell lines including HEK239T, Hela, HepG2, U87, but we can use other cell lines according to your requirements.
➢ Blood Lineage Cells (RAW264.7, HMC1.2, K562, U937 etc.)
➢ Cancer Cell Lines (HEK293, HEK293T, Hela, MCF7, Neuro2a, HepG2, U87 etc.)
➢ Stem Cells (iPSC)
➢ Other Cell Lines (NIH3T3, MCF10, HEME, SW10 etc.)
CRISPR/Cas9 PlatformCB also has extensive experience in incorporating CRISPR/Cas9 technology into animal models, which have been fully recognized by our clients. Tell us your needs, we provide a one-stop-shop DKK1 CRISPR/Cas9 gene editing animal service and guarantee at least 2 founders or 3 F1 animals with shorter turnaround time and lower price. Our DKK1 gene editing animal model generation services include:
➢ DKK1 gene conventional knockout animals
➢ DKK1 gene conditional knockout animals
➢ DKK1 point mutation animals
➢ DKK1 knockin animals
Alternative species: mouse, rat, rabbit, zebrafish, C. elegans, etc.
CRISPR/Cas9 PlatformCB is devoted to providing the best gene editing services and products for academic research, biotech research and pharmaceutical drug discovery with excellent quality management and quality assurance capacity. To accelerate the achievement of your research goals, our gene editing expert team provides you with custom CRISPR/Cas9 services for any specific gene to help you solve problems encountered during your research. If you have any question, please feel free to contact us.
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