Gene: PMEL
Official Full Name: premelanosome proteinprovided by HGNC
Gene Summary: This gene encodes a melanocyte-specific type I transmembrane glycoprotein. The encoded protein is enriched in melanosomes, which are the melanin-producing organelles in melanocytes, and plays an essential role in the structural organization of premelanosomes. This protein is involved in generating internal matrix fibers that define the transition from Stage I to Stage II melanosomes. This protein undergoes a complex pattern of prosttranslational processing and modification that is essential to the proper functioning of the protein. A secreted form of this protein that is released by proteolytic ectodomain shedding may be used as a melanoma-specific serum marker. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35433 | PMEL Knockout cell line (HeLa) | Human | PMEL | 1:3~1:6 | Negative | Online Inquiry |
KO35434 | PMEL Knockout cell line (HCT 116) | Human | PMEL | 1:2~1:4 | Negative | Online Inquiry |
KO35435 | PMEL Knockout cell line (HEK293) | Human | PMEL | 1:3~1:6 | Negative | Online Inquiry |
KO35436 | PMEL Knockout cell line (A549) | Human | PMEL | 1:3~1:4 | Negative | Online Inquiry |
PMEL Gene Knockout Cell Lines are advanced genetic models designed to facilitate the study of the PMEL gene, which is essential for melanin biosynthesis and plays a significant role in the development of melanocytes. These cell lines are engineered using CRISPR/Cas9 technology to ensure precise and complete knockout of the PMEL gene, thereby enabling researchers to investigate its specific functions and mechanisms in various biological processes. By eliminating the PMEL gene, these cell lines serve as a critical tool for elucidating the molecular pathways involved in pigment formation and related disorders.
The primary function of PMEL Gene Knockout Cell Lines is to provide an experimental platform that mimics the absence of the PMEL protein, allowing scientists to assess the subsequent alterations in melanin production and cellular behavior. The knockout model enables detailed investigations into the role of PMEL in pigmentary diseases, cellular stress responses, and other melanocyte-related functions. Additionally, these cell lines can be utilized in drug discovery and therapeutic research aimed at pigmentary conditions, enhancing their relevance in translational research.
The scientific importance of PMEL Gene Knockout Cell Lines lies in their application across both research and clinical settings. In research, they offer unparalleled insights into the genetic and molecular basis of pigmentation and various skin disorders, while providing a platform for testing novel therapeutics. Clinically, these cell lines can aid in developing targeted treatments for conditions such as vitiligo and melanoma, thus bridging the gap between basic science and clinical application.
Compared to alternative models, such as wild-type cell lines or less targeted gene editing approaches, PMEL Gene Knockout Cell Lines offer precise gene modulation with reduced off-target effects, ensuring that findings are both reliable and reproducible. Their specificity allows researchers to gain more profound insights into PMEL-related pathways without the confounding influence of other genetic factors.
For researchers, clinicians, and biotechnology developers, PMEL Gene Knockout Cell Lines represent an invaluable asset in the pursuit of understanding and treating pigment-related disorders. The capacity for detailed genetic analysis and drug testing makes these lines a cornerstone of innovative biological research. With a commitment to cutting-edge solutions, our company provides these high-quality knockout cell lines, backed by extensive expertise in genetic engineering and cellular biology, ensuring that you have the best tools at your disposal for your research endeavors.
Please note that all services are for research use only. Not intended for any clinical use.
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