Fig. S3.a

Aug 15, 2014

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Fig. S3.a. Fig. S3.b.

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Fig. S3.a

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Fig. S3.a Fig. S3.b

FIG 601 A

FIG 601 A. VALVE SUB, SHIFT. P1. 198. FIG 601B. VALVE SUB , MAIN. P1. 200. FIG 601C. VALVE SUB , MAIN ( OPTION :AQ ). P1. 202. FIG 602. DRAWBAR ASSY. P1. 204. FIG 603A. FILTER SUB, SUCTION. P1. 206. FIG 603B. GEAR PUMP ASSY. P1. 208. FIG 604. CASE , CYLINDER. P1. 210.

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Building a Database on S3

Building a Database on S3. Matthias Brantner , Daniela Florescu , David Graf, Donald Kossmann , Tim Kraska Xiang Zhang 2014-04-10. Outline. Introduction What is AWS Using S3 as a disk Basic commit protocols Transactional properties Experiments and results

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Fig S3

Class II. Class I. Fig S3.

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S3.

S3. a. Mice subsequentlly used for testing… PSGL1 Fc -control non-modified. b. c. Nuclei stained with DAPI PSGL1 staining of endothelium.

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Fig. S6 a

Fig. S6 a.

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Figure S3

Figure S3.

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Fig. S1.a

Fig. S1.a. Fig. S1.b.

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Fig. S3

Fig. S3. PMM. PMT. green. purple. cyan. turquoise. turquoise. pink. magenta. greenyellow. black. red. royalblue. pink. white. midnightblue. turquoise. drakgreen. darkgreen. grey60. lightyellow. purple. brown. midnightblue. greenyellow. green. darkturquoise. yellow.

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S3 Admin

S3 Admin. 3 Units. Admin Services ITFA PCI.

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Fig. S3

HNSC #1. HNSC #2. CD44(-). CD44(+). CD44(-). CD44(+). OCT4 DAPI. OCT4 DAPI. OCT4 DAPI. OCT4 DAPI. SOX2 DAPI. SOX2 DAPI. SOX2 DAPI. SOX2 DAPI. Fig. S3.

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Fig. 47.1 (a)

Organic compounds possessing different functional groups usually have different physical and chemical properties. Chloroethane (CH 3 CH 2 Cl ). Fig. 47.1 (a) Chloroethane is a gas at room conditions. It is largely used as a blowing agent in foamed plastics. Ethanol (CH 3 CH 2 OH ).

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Supplementary Fig. A

AFLP. 100. 20. 30. 40. 50. 60. 70. 10. 80. 90. 0. CCBAU23115. CCBAU43229. 1. CCBAU33191. CCBAU43241. CCBAU23116. CCBAU65311. CCBAU65310. CCBAU53093-1. CCBAU53093-2. CCBAU43230. USDA 2370 T. 2. CCBAU23122. CCBAU23127. CCBAU33201. CCBAU23132. CCBAU23123. CCBAU33202.

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S3 IETD

Supplemental Data Figure 2. 20. 15. Apoptotic cells (%). 10. 5. WT. S3. S3 IETD. S3 ZB4. S3 CH11. S3 CH1 IETD. S3 CH11 ZB4. S3 DMSO.

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Supplementary Fig S3

A. MCF-7EpiR. MCF-7TaxR. siControl. siSIRT6. siControl. siSIRT6. Paclitaxel ( h ):. Epirubicin ( h ). 0. 24. 48. 0. 24. 48. 0. 48. 72. 0. 48. 72. SIRT6. SIRT6. FOXO3a. FOXO3a. p27Kip1. p27Kip1. H3K9ac. Ac-p53. H3K56ac. p53. H3K9Ac. Ac-α-TUBULIN. H3K56Ac.

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Fig. S3

A. B. C. D. E. Fig. S3. Fig. S3 Stability of the variegated phenotype. All mice depicted in this Figure were derived from the Tg shA57.2-1 strain and were assayed by flow cytometry as described in the legend to Fig. 2.

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Figure S3

A. 16. 24. 48. 72. 96. 16. 24. 48. 72. 96. 4. 24. 48. 72. B. C. HL60. K562. VitD3. RA. Ara-C. CTR. CTR. hrs. hrs. -NFIA. -NFIA. -CEBP a. -CEBP a p42. *. -CEBP b LAP. -CEBP a p30. -CEBP b LIP. -CEBP b LAP. -PU.1. -CEBP b LIP. -GATA1. -LMO2. -PU.1. -TAL1.

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Fig. S3

Fig. S3.

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Fig. S3

Fig. S3. a. b. c.

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Fig. S4.a

Fig. S4.a. Fig. S4.b.

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Fig. S2.a

Fig. S2.a. Fig. S2.b.

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Fig. S3 The Zeta potential (ξ) distribution curve of AuNR@Cysteamine .

Fig. S1. The VSM plot of Gd 2 O 3 : Eu@MPA Lanthanide nanophosphor taken at Room Temperature. Fig. S2 The Zeta potential (ξ) distribution curve of Gd 2 O 3 : Eu@MPA Lanthanide nanophosphor. Fig. S3 The Zeta potential (ξ) distribution curve of AuNR@Cysteamine.

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FIG 601 A

FIG 601 A. PIPE , FORWARD/REVERSE. P1. 198. FIG 601B. VALVE SUB , MAIN. P1. 200. FIG 602. DRAWBAR ASSY. P1. 204. FIG 603A. FILTER SUB, SUCTION. P1. 206. FIG 603B. GEAR PUMP ASSY. P1. 208. FIG 604. CASE , CYLINDER. P1. 210. FIG 605. ARM SUB, LIFT MAIN CONTROL VALVE SUB.

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