Gene: CPXCR1
Official Full Name: CPX chromosome region candidate 1provided by HGNC
Gene Summary: This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA09282 | CPXCR1 Knockout cell line (AC16) | Human | CPXCR1 | 1:3-1:4 | negative | Online Inquiry |
| KOA24728 | CPXCR1 Knockout cell line (BEAS-2B) | Human | CPXCR1 | 1:3~1:4 | negative | Online Inquiry |
| KOA40175 | CPXCR1 Knockout cell line (U-2932) | Human | CPXCR1 | 1:2-1:4 | negative | Online Inquiry |
| KOA55563 | CPXCR1 Knockout cell line (TPC-1) | Human | CPXCR1 | 1:5-1:8 | negative | Online Inquiry |
| KOA70981 | CPXCR1 Knockout cell line (NCM460) | Human | CPXCR1 | 1:2~1:3 | negative | Online Inquiry |
Please note that all services are for research use only. Not intended for any clinical use.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.