Detection method details
Name: |
QL-CON-35S166-F/hpt166-R |
Description: |
Qualitative real-time PCR (TaqMan) method for detection of the junction between the CaMV 35S promoter and the hpt gene (Reiting et al., 2010). |
Comment: |
Target is the junction region between the Cauliflower mosaic virus (CaMV) 35S promoter (P-35S) and the hygromycin phophotransferase II (hpt) gene. |
Validation: |
unknown |
Standardisation: |
none |
Related Methods: |
Type: |
construct-specific |
Target GMO names: |
Kefeng6
|
-
Oligonucleotides:
Forward Primer
Name:
35S166-FSequence:
GCTGAAATCACCAGTCTCTCTCTACASize:
26
Reverse Primer
Name:
hpt166-RSequence:
TGAGTTCAGGCTTTTTCATATCTCATSize:
26
Probe
Name:
35S166-TmSequence:
TATCTCTCTCGAGCTTTCGCAGATCCGGSize:
28
-
Amplicon:
Sequence:
Size:
90
Documents
| Citation | Type | Local copy |
|---|---|---|
Sampling and analysis guidelines for the detection of genetic modifications in rice![]() |
PCR Protocol |
Download PDF
![]() |
Reiting R, Grohmann L, Maede D (2010) A testing cascade for the detection of genetically modified rice by real-time PCR in food and its application for detection of an unauthorized rice line similar to KeFeng6. J. Verbr. Lebensm. 5:185-188![]() |
peer-reviewed article |
Download PDF
![]() |
| Protocol QL-CON-35S166-F/hpt166-R | PCR Protocol |
Download PDF
![]() |


