ライフサイエンスコーパス: radioiodination

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1 ody was also labeled using the residualizing radioiodination agent N-succinimidyl 4-guanidinomethyl-3

2 ontrast to non site-specific methods such as radioiodination, antibodies labeled with casein kinase I

3 The radioiodination (I-125) of one congener member (4-[125I]

4 and without a cell surface cross-linker and radioiodination in conjunction with immunoprecipitation

5 Radioiodination of [123I]IQNB from our tri-n-butylstanny

6 olabeling and purification for the scaled-up radioiodination of a humanized anti-carcinoembryonic ant

7 est that SIPC is a promising reagent for the radioiodination of anti-EGFRvIII L8A4 and, possibly, oth

8 The method was also modified for the radioiodination of arenes using a one-pot procedure invo

9 Rapid and efficient radioiodination of aryl and heteroaryl bromides has been

10 e with different labeling procedures for the radioiodination of benzamides and report on initial dosi

11 that D-KRYRR is a promising reagent for the radioiodination of internalizing mAbs, such as the anti-

12 ope ([*I]SIB), which is an agent used in the radioiodination of proteins and peptides, from its tin p

13 Radioiodination of the purified OST reveals that DAD1 is

14 Radioiodination of the substance P analogs resulted in t

15 Following radioiodination of the TPP-based prosthetic group in pho

16 yridinecarboxylate (SIPC) might be ideal for radioiodination of these mAbs because of the positive ch

17 Radioiodination of tubulysins was 92% to 98% efficient a

18 (131)I-radioiodination of two synthetic tubulysin A analogues,

19 Capsid radioiodination of viral vectors enables non-invasive, w

20 Radioiodinations of the peptides followed by conjugation

21 We report a rapid (5 min) and simple radioiodination procedure for preparing [123I]IQNB from

22 The objective of this study was to develop a radioiodination procedure primarily to assess PET imagin

23 Unfortunately, cumbersome and inefficient radioiodination procedures have limited the practicality

24 , another residualizing agent, and by direct radioiodination using IODO-GEN ((125)I-Nanobody).

25 Radioiodination via an indirect method attenuated uptake

26 When direct radioiodination was performed with conventional methods,

27 potential of anti-HER2 5F7GGC Nanobody after radioiodination with the residualizing agent N-succinimi

28 thesized and conditions were established for radioiodination with yields of approximately 70% for 131

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