Receptor Tyrosine Kinase (RET) Mutant (D4) Aptamer Details
ID# 7500
Structure
Chemistry
2'-F-RNA
Target
Receptor Tyrosine Kinase (RET) Mutant
Category
Protein
Affinity (Kd)
35 nM
Length
50
Aptazyme
No
Sequence (3-char table code)
G
A
C
U/T
5'-rGpfCprGpfCprGprGprGprAprApfUprAprGpfUprApfUprGprGprAprAprGprGprApfUprApfCprGpfUprApfUprApfCpfCprGpfUprGpfCprAprApfUpfCpfCprAprGprGprGpfCprAprApfCprGp-3'
Molecular Weight: 16281.84
Extinction Coefficient: 511900
Binding Conditions / Buffer
Selection buffer: RPMI 1640
Binding Temp: 37°C
Refolding Protocol
If the oligo is a known aptamer sequence: For binding studies, perform a refolding protocol to ensure proper function (i.e. binding to antigen or target). Refer to the aptamer reference source for the appropriate refolding parameters and binding conditions. Note: it is unknown whether aptamer functions properly without refolding.
Note: Information on this aptamer oligo was obtained from the literature and hasn't been validated by Aptagen.
Reference
Cerchia, Laura, et al. "Neutralizing Aptamers from Whole-Cell SELEX Inhibit the RET Receptor Tyrosine Kinase." PLoS Biology, 3 (2004): e123
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