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Table 1 Primers used for shark VNAR library construction and sequencing

From: Isolation and characterization of malaria PfHRP2 specific VNAR antibody fragments from immunized shark phage display library

Primers description

Nucleotide sequence (5′→3′)

Applications

Leader-F

ATGAATATTTTCTTGCYGTCAGTCC

1st PCR

C-DomainR

CCTCTCTGTTCTTCRGTTGCAGAGT

1st PCR

FR1F1

RCAWGGGTRGACCAAACACC

Nested PCR

FR4R

TTTCACGGTYARTRCGGTGCC

Nested PCR

T7SelectUP (For)

GGAGCTGTCGTATTCCAGTC

T7 Phage sequencing

T7SelectDOWN (Rev)

AACCCCTCAAGACCCGTTTA

T7 Phage sequencing

T7Seq_For

TAATACGACTCACTATAGGG

pET vector sequencing forward

T7Seq_Rev

CTAGTTATTGCTCAGCGGTG

pET vector sequencing reverse

  1. Association (ka), dissociation rates (kd), and equilibrium constants (KD) of mAbs D2, F9, and C1–13 against rPfHRP2. The analysis for mAbs D2 and F9 were undertaken using the Octet Red platform, whereas mAb C1–13 was determined by BIAcore