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Traditional Transgenic Services
Traditional Transgenic Services

Traditional C. elegans Transgenic services

Traditional transgenic services include generating extrachromosomal arrays and integrated arrays. These services will generate transgenic animals with multiple-copy transgenes, and result in over expression of the target plasmid.

These services begin from the microinjection of the DNA mixture into C. elegans gonads to generate extrachromosomal transgenic arrays that contain high copy numbers of the injected DNA constructs. For the X-ray mediated integrated arrays, the extrachromosomal arrays will be treated with X-ray irradiation, and screened for integrated arrays. The integration site is random and could be determined by mapping.

  • SunyBiotech c.elegans generating extrachromosomal arrays and X-ray induced integrated arrays
  • SunyBiotech c.elegans generating extrachromosomal arrays and X-ray induced integrated arrays
  • SunyBiotech c.elegans generating extrachromosomal arrays and X-ray induced integrated arrays
  • SunyBiotech c.elegans generating extrachromosomal arrays and X-ray induced integrated arrays
  • SunyBiotech c.elegans generating extrachromosomal arrays and X-ray induced integrated arrays
  • SunyBiotech c.elegans generating extrachromosomal arrays and X-ray induced integrated arrays
  • SunyBiotech c.elegans generating extrachromosomal arrays and X-ray induced integrated arrays
  • SunyBiotech c.elegans generating extrachromosomal arrays and X-ray induced integrated arrays

Figure 1    Schematic diagram of generating extrachromosomal arrays and X-ray induced integrated arrays


Plasmid Construction

Vector modifications (replacement of promoter, coding sequence or 3' UTR sequence), sub-cloning and site-directed mutagenesis are common techniques used in molecular biology experiments. SunyBiotech can provide efficient vector modification, sub-cloning, and site-directed mutagenesis service based on customers' needs. Moreover, we can do vector modifications using a ligation-independent method. Therefore, no additional restriction enzyme sites or linker sequences will be added.


PIDServiceYou need to provideTurnaround(wk)Price(US$)Deliverables
C001Plasmid Construction

1. Information of the vector backbone

2. The modification you need

2-3Starts from 200 USD*Plasmid and sequencing reports
B001Extra-chromosomal arrays
  1. 1. Target plasmid and it's concentration
  2. 2. The marker and it's concentration
  3. 3. Background strain information
3-4
500 USD(≥3 lines)Extrachromosomal lines that contain the target plasmid and report markers
B002X-ray mediated integrated arrays8-101049 USD(1 line)Integrated lines that contain the target plasmids and report markers


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