Table S1. Primers used for semiquantitative RT-PCR

Table S1. Primers used for semiquantitative RT-PCR

4 4 10 10 3 3 10 10 93.4 96.6 2 2 10 10 1 1 10 10 0 0 10 10 0 1 2 3 4 0 1 2 3 4 10 10 10 10 10 10 10 10 10 10 Fig. S1. Representative flow cytometric profiles with the ratio of mouse and human macrophages after the induction of macrophages as described in Material and methods. Human macrophages Mouse peritoneal macrophages CD56 CD49b CD11b CD14

Fig. S2. Anti-CD47 Ab did not inhibit the proliferation of PEL cells. PEL cell lines (BCBL-1, BC-2 and BCP-1) were incubated with 0, 0.3, 1, 3, 10 µg/ml anti-CD47 Ab for 72 h. A cell proliferation assay was carried out using MTT as described in Material and methods. Cell viability(%) Anti-CD47 Ab (μg/ml)

Table S1. Primers used for semiquantitative RT-PCR

Table S1. Primers used for semiquantitative RT-PCR

Presentation Transcript

Supplementary data Table 1. PCR primers used to amplify TP53 Exons from genomic DNA

Supplemental table 1 : List of primers used for Me-DIP coupled Q-PCR.

RT-PCR lab

Supplementary Table S1. List of oligonucleotide primers used for amplification

Supplementary Material 2. PCR primers used in this study.

TABLE 5. Sequence of Primers used.

Table S1 List of primers used for PCR and qPCR analyses

RT-PCR for NMDAR 1

Supplementary Table I . Gene-specific primers used for quantitatative real-time PCR

Supplementary Table 2: Nucleotide sequence of primers used for PCR amplification

Additional file 4 – Primers used for PCR analysis of transformants

Table S1. Organisms used for lytA specificity studies

Supplementary table 1: Primers used for PCR amplification

Table S1. Primers and Probes Used in RT-PCR and qMSP

Supplementary Table 1 . List of primers used for real-time PCR analysis

Supplementary Table 1 Sequences of quantative RT-PCR primers

RT-PCR

TABLE S1. Primers used in mutagenesis of Q motif of FANCJ and BLM

Table S2. Sequences of primers used for RT-PCR

Supplementary table S1: PCR conditions for 5’RACE analysis.

RT-PCR