GMO Corn Screen-1 Real-TM Real Time PCR kit for detection of MON810, NK-603, T-25
-
Catalog number
R-G4-L1-50FRT
-
Price
Please ask
-
Size
50 Tests
-
-
PCR for diagnosis
This GMO Corn Screen-1 Real-TM Real Time PCR kit for detection of MON810, NK-603, T-25 is used as PCR kit for molecular diagnostics with elecrtophoresis, qPCR or real-time PCR of 50 Tests per screening.
-
-
ISO CE marked fro IVD
This molecular diagnostic PCR kit is CE approved and complies with the Directive 98/79/EC for IVD, in vitro PCR Diagnostics. The PCR kit is ISO 9001:2008 and ISO 13485:2012, CE marked with the in vitro diagnostic medical divices requirements Annex 2 of list B of the laboratory Directive 98/79/EC and can be used for diagnosis of viruses. The kit inculde all reagents for PCR or RT-PCR of viral DNA or RNA.
-
-
Description
The detections of the targets with this kit is a type of test that can be performed on any target containing biological samples after clean up of interfering agents. The assay must be performed following the protocol. GMO maize, corn , soybean detection and PCR screening for a genetically modified organism (GMOs) . GMOs are the source of medicines and genetically modified foods and are widely used . The term GMO is defined in the Cartagena Protocol on Biosafety, which regulates international trade in living GMOs. Most used are PCR GMO detection kits.
-
Group
PCR, polymerase chain reaction
-
About
TAQ or Pfu or Pfx or other enzymes are used for polycmerase chain reaction and have different specificity. The mores specific the lower the yield.
-
Properties
Thermocyclers can be callibrated for identical ramping curves to obtain a more accurate PCR.
-
Gene target
-
Gene symbol
MT-TM, TSPAN16, ACP3, P4HTM, SNORD116-25, ZNF211, SNORD114-25, SNORD115-25, TBXT, PLS3
-
Short name
Corn Screen-1 Real-TM Real Time PCR kit for of MON810, NK-603, T-25
-
Technique
detection, PCR, The polymerase chain reaction (PCR) amplifies the DNA in your sample. For real time PCR the cycle threshold Ct values willneed to be set before the experiment. Than the RT-PCR starts from RNA and real time PCR quantitates the cDNA so the RNA in the sample on given time of the experiment.
-
Alternative name
GMO Corn Screen-1 Real-TM Quantitative real-time PCR test kit reagent to measure quantification on MON810, NK-603, T-25
-
Alternative technique
kits, dna-amplification
-
Alternative to gene target
v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog, C-Kit and CD117 and PBT and SCFR, KIT and IDBG-18980 and ENSG00000157404 and 3815, transferase activity, Extracellular, Kit and IDBG-172083 and ENSMUSG00000005672 and 16590, KIT and IDBG-642326 and ENSBTAG00000002699 and 280832
-
Gene info
Gene info
-
Identity
-
Gene
-
Long gene name
tetraspanin 16
-
Synonyms gene
-
Synonyms gene name
- transmembrane 4 superfamily member 16
-
Synonyms
-
GenBank acession
-
Locus
-
Discovery year
2004-10-19
-
Entrez gene record
-
Pubmed identfication
-
RefSeq identity
-
Classification
-
VEGA ID
Gene info
-
Identity
-
Gene
-
Long gene name
acid phosphatase 3
-
Synonyms gene
-
Synonyms gene name
- acid phosphatase, prostate
-
Synonyms
-
Synonyms name
-
Locus
-
Discovery year
1989-05-30
-
Entrez gene record
-
Pubmed identfication
-
RefSeq identity
-
Classification
-
VEGA ID
Gene info
Gene info
Gene info
-
Identity
-
Gene
-
Long gene name
zinc finger protein 211
-
Synonyms
-
GenBank acession
-
Locus
-
Discovery year
1999-09-29
-
Pubmed identfication
-
Classification
-
VEGA ID
Gene info
Gene info
Gene info
Gene info
-
Identity
-
Gene
-
Long gene name
plastin 3
-
Synonyms gene name
-
Synonyms
-
GenBank acession
-
Locus
-
Discovery year
1997-08-18
-
Entrez gene record
-
Pubmed identfication
-
Classification
- EF-hand domain containing
-
VEGA ID
-
Locus Specific Databases
MeSH Data
-
Name
-
Concept
Scope note:
In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
-
Tree numbers
-
Qualifiers
ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
Similar products
