<p>Sites for restriction enzymes BamHI (GGATCC), XhoI (CTCGAG), XbaI (TCTAGA) and EcoRV (GATATC) are shown underlined. Stop codons are shown in bold, either in the 5′ to 3′ (TAA) or 3′ to 5′ (TTA) orientation. The third column indicates which peptide fragments each primer was used to construct, or where the primer was used to clone the heavy and light chain variable regions of F1-40. Primers used only for sequencing are indicated by the abbreviation “seq.”</p
a<p>Nucleotides in bold represent restriction enzyme sites added to the 5′ region of the primer.</p>...
a<p>The sequence in boldface type is the EcoRI restriction enzyme site.</p>b<p>The sequence in boldf...
<p>a. Introduced restriction sites are underlined. Amino acid spacer (GGGS) at the N-terminus of GFP...
<p>Sites for restriction enzymes BamHI (GGATCC), XhoI (CTCGAG), are shown underlined. Stop codons ar...
<p><sup>a</sup> Underlined sequences correspond to restriction enzyme sites introduced for cloning p...
<p><sup>a</sup> The underlined sequences are restriction enzyme sites: a BamHI site (P3F), NdeI site...
a<p>The underlined sequences are restriction enzyme sites: <i>Acc</i>65I sites (P1F and P7F), <i>Bam...
a<p>When relevant, primer attachment sites are indicated in bold. Relevant restriction enzyme sites ...
a<p>For each truncation construct, forward primer (F) is in the forward orientation relative to the ...
<p>Sequences recognized by restriction enzymes (in parentheses) are underlined. The start and stop c...
<p>Underlined regions represent restriction enzyme sequences</p><p>Primers and probes used in this s...
a<p>The areas underlined correspond to restriction enzyme sites used and the base underlined and bol...
<p>Wt: Wild-type; Mut: mutant; F: Forward primer; R: Reverse primer. The sequences of restriction si...
Primers used in this study(underlined in the primer sequences were restriction enzyme sites).</p
1<p>Underlined letters highlight engineered restriction enzyme (RE) sites (names of the introduced R...
a<p>Nucleotides in bold represent restriction enzyme sites added to the 5′ region of the primer.</p>...
a<p>The sequence in boldface type is the EcoRI restriction enzyme site.</p>b<p>The sequence in boldf...
<p>a. Introduced restriction sites are underlined. Amino acid spacer (GGGS) at the N-terminus of GFP...
<p>Sites for restriction enzymes BamHI (GGATCC), XhoI (CTCGAG), are shown underlined. Stop codons ar...
<p><sup>a</sup> Underlined sequences correspond to restriction enzyme sites introduced for cloning p...
<p><sup>a</sup> The underlined sequences are restriction enzyme sites: a BamHI site (P3F), NdeI site...
a<p>The underlined sequences are restriction enzyme sites: <i>Acc</i>65I sites (P1F and P7F), <i>Bam...
a<p>When relevant, primer attachment sites are indicated in bold. Relevant restriction enzyme sites ...
a<p>For each truncation construct, forward primer (F) is in the forward orientation relative to the ...
<p>Sequences recognized by restriction enzymes (in parentheses) are underlined. The start and stop c...
<p>Underlined regions represent restriction enzyme sequences</p><p>Primers and probes used in this s...
a<p>The areas underlined correspond to restriction enzyme sites used and the base underlined and bol...
<p>Wt: Wild-type; Mut: mutant; F: Forward primer; R: Reverse primer. The sequences of restriction si...
Primers used in this study(underlined in the primer sequences were restriction enzyme sites).</p
1<p>Underlined letters highlight engineered restriction enzyme (RE) sites (names of the introduced R...
a<p>Nucleotides in bold represent restriction enzyme sites added to the 5′ region of the primer.</p>...
a<p>The sequence in boldface type is the EcoRI restriction enzyme site.</p>b<p>The sequence in boldf...
<p>a. Introduced restriction sites are underlined. Amino acid spacer (GGGS) at the N-terminus of GFP...