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1 development of new synthetic methodology for radioiodination.
2 ody was also labeled using the residualizing radioiodination agent N-succinimidyl 4-guanidinomethyl-3
3 ontrast to non site-specific methods such as radioiodination, antibodies labeled with casein kinase I
4                                          The radioiodination (I-125) of one congener member (4-[125I]
5  and without a cell surface cross-linker and radioiodination in conjunction with immunoprecipitation
6                                              Radioiodination of [123I]IQNB from our tri-n-butylstanny
7 olabeling and purification for the scaled-up radioiodination of a humanized anti-carcinoembryonic ant
8 est that SIPC is a promising reagent for the radioiodination of anti-EGFRvIII L8A4 and, possibly, oth
9         The method was also modified for the radioiodination of arenes using a one-pot procedure invo
10                          Rapid and efficient radioiodination of aryl and heteroaryl bromides has been
11 e with different labeling procedures for the radioiodination of benzamides and report on initial dosi
12  that D-KRYRR is a promising reagent for the radioiodination of internalizing mAbs, such as the anti-
13 ope ([*I]SIB), which is an agent used in the radioiodination of proteins and peptides, from its tin p
14                                              Radioiodination of the purified OST reveals that DAD1 is
15                                              Radioiodination of the substance P analogs resulted in t
16                                    Following radioiodination of the TPP-based prosthetic group in pho
17 yridinecarboxylate (SIPC) might be ideal for radioiodination of these mAbs because of the positive ch
18                                              Radioiodination of tubulysins was 92% to 98% efficient a
19                                       (131)I-radioiodination of two synthetic tubulysin A analogues,
20                                       Capsid radioiodination of viral vectors enables non-invasive, w
21                                              Radioiodinations of the peptides followed by conjugation
22         We report a rapid (5 min) and simple radioiodination procedure for preparing [123I]IQNB from
23 The objective of this study was to develop a radioiodination procedure primarily to assess PET imagin
24    Unfortunately, cumbersome and inefficient radioiodination procedures have limited the practicality
25 , another residualizing agent, and by direct radioiodination using IODO-GEN ((125)I-Nanobody).
26                                              Radioiodination via an indirect method attenuated uptake
27                                  When direct radioiodination was performed with conventional methods,
28 potential of anti-HER2 5F7GGC Nanobody after radioiodination with the residualizing agent N-succinimi
29 thesized and conditions were established for radioiodination with yields of approximately 70% for 131