BioLit FluroGreen qPCR Master Mix (Low CAR) (2X)
-
Catalog number78797
-
PricePlease ask
-
Size0.5 ml
-
-
Reagent propertiesMolecular biology DNA amplification enzymes and reagents
-
PropertiesMaster mixes of Taq polymerases are supplied with dNTP's and Mg+buffer already premixed. They are used for automation and to exclude variaions in your PCR.
-
Gene target
-
Gene symbolCXADR, CXADRP1, NR1I3, SPG7
-
Short nameBioLit FluroGreen qPCR Master ( CAR) (2X)
-
Alternative nameBioLit FluroGreen Quantitative real-time PCR test kit Master Mix (Low CAR) (2X)
-
Gene info
-
Identity
-
Gene
-
Long gene nameCXADR Ig-like cell adhesion molecule
-
Synonyms gene name
- coxsackie virus and adenovirus receptor
- CXADR, Ig-like cell adhesion molecule
-
Synonyms
-
GenBank acession
-
Locus
-
Discovery year1998-03-24
-
Entrez gene record
-
Pubmed identfication
-
Classification
- IgCAM CXADR-related subfamily
- V-set domain containing
-
VEGA ID
Gene info
-
Identity
-
Gene
-
Long gene nameCXADR pseudogene 1
-
Synonyms gene name
- coxsackie virus and adenovirus receptor pseudogene 1
-
Synonyms
-
Locus
-
Discovery year2008-01-31
-
Entrez gene record
-
VEGA ID
Gene info
-
Identity
-
Gene
-
Long gene namenuclear receptor subfamily 1 group I member 3
-
Synonyms gene name
- nuclear receptor subfamily 1, group I, member 3
-
Synonyms
-
Synonyms name
-
GenBank acession
-
Locus
-
Discovery year1999-09-23
-
Pubmed identfication
-
Classification
- Nuclear receptor subfamily 1 group I
-
VEGA ID
Gene info
-
Identity
-
Gene
-
Long gene nameSPG7 matrix AAA peptidase subunit, paraplegin
-
Synonyms gene
-
Synonyms gene name
- cell matrix adhesion regulator
- spastic paraplegia 7 (pure and complicated autosomal recessive)
-
Synonyms
-
Synonyms name
-
GenBank acession
-
Locus
-
Discovery year1998-06-25
-
Entrez gene record
-
Pubmed identfication
-
RefSeq identity
-
Classification
- AAA ATPases
-
VEGA ID
-
Locus Specific Databases
MeSH Data
-
Name
-
ConceptScope 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
- E05.393.620.500
-
Qualifiersethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data