AA Mutation: p.C176F
Nucleotide Mutation: c.527G>T
dPCR wet-lab validated
Nucleotide Mutation: c.527G>T
dPCR wet-lab validated
Assay Name​
dPCR Mutation Assay TP53 10645 Human
GeneGlobe Cat No (Assay ID)​
DMH0000353
Species​
Human (Homo sapiens)
Gene Symbol​
TP53
Gene aliases​
p53;LFS1
Ensembl Gene ID​
ENSG00000141510
Entrez Gene ID​
7157
Genomic Mutation ID (COSV by COSMIC)​
COSV52661329
Legacy Mutation ID (COSM by COSMIC)​
COSM10645
Amino Acid Change​
p.C176F
Nucleotide Change​
c.527G>T
Wildtype Allele​
C
Mutant Allele​
A
Mutation Strand​
-
Mutant description​
Substitution - Missense
Positive Control Sequence​
CCCCAGCTGCTCACCATCGCTATCTGAGCAGCGCTCATGGTGGGGGCAGCGCCTCACAACCTCCGTCATGTGCTGTGACTGCTTGT
Amplicon length​
66
Recommended Restriction Enzyme​
CviQI,AluI,HaeIII,EcoRI,XbaI,PvuII
Wet-lab validated​
dPCR wet-lab validated
Probe Fluorophore​
FAM/HEX, ATTO550/ROX or Cy5/ATTO700
Quencher​
Iowa Black
Primer Purification​
Desalted
Probe Purification​
HPLC
Reaction size​
200rxns and 1000rxns