User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/12 - Revision history

Keyun Wang at 16:07, 5 October 2012

Keyun Wang — Fri, 05 Oct 2012 16:07:22 GMT

←Older revision		Revision as of 16:07, 5 October 2012
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	==Purpose==		==Purpose==
	* To check if solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced fibers		* To check if solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced fibers
-	* To mix supernatant ~~of sample~~ with ~~fiber~~ pellet with different concentration of Tris buffer at pH 10 and check re-suspension	+	* To mix supernatant with pellet in each sample with the addition of different concentration of Tris buffer at pH 10 and check re-suspension
-	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:55, 17 September 2012 (EDT)''':I'm confused by this. are you adding tris to the pelletonly, to just the supernatant or to both?	+
-	* Prepare the ratio 80 Au/BSA sample for peak shift testing next week	+
-	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:55, 17 September 2012 (EDT)''':explain what hte peak shift experiemnt is.	+

	==Procedure==		==Procedure==
-	* Sets of Au/BSA solutions with different ratios were remade from ratio 80 to ratio 170. For details with the volume, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]]. The sets of solutions were incubated in 85°C for four hours. After four hours of incubation, 1mL of supernatant were measured for absorption activity under UV-vis from 700nm to 200nm. ~~For details of the results, see~~ [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]].	+	* Sets of Au/BSA solutions with different ratios were remade from ratio 80 to ratio 170. For details with the volume, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]]. The sets of solutions were incubated in 85°C for four hours. After four hours of incubation, 1mL of supernatant were measured for absorption activity under UV-vis from 700nm to 200nm. See [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for details on absorption of each Au/BSA solutions after 4 hours of incubation.
-	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''':masses and volumes and ratios. can reference the calculations and precise details ~~are in Dhea's notebook~~.	+	* 100mM Tris buffer at pH 10 were diluted to 50mM Tris buffer at pH 10 with distilled water. 1M Tris buffer were made, pH were adjusted to pH 10 with the addition of 1M HCl as stock solution stored in fridge. 500mM Tris buffer at pH 10 were made by diluting from 1M Tris buffer. Please refer to [[User:Melissa Novy/Notebook/CHEM-571/2012/09/12\|Melissa's Notebook]] for details on the calculation on the actual and theoretical mass and concentration obtained for 100mM Tris buffer.
-	* 100mM Tris buffer at pH 10 were diluted to 50mM Tris buffer at pH 10 with distilled water. 1M Tris buffer were made, pH were adjusted to pH 10 with the addition of 1M HCl as stock solution stored in fridge. 500mM Tris buffer at pH 10 were made by diluting from 1M Tris buffer.	+	* Absorbency were measured using UV-vis spectrometer for the sets of Au/BSA samples made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]]. 1mL of each sample were used for measurement. For details of the absorbance, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for the absorbance obtained for Au/BSA sample after 4 hours of incubation.
-	*'''[[User:~~Abigail E. Miller~~\|~~Abigail E. Miller~~]] ~~10:58, 17 September 2012 (EDT)''':masses and volumes and ratios. can reference~~ the ~~calculations~~ and ~~rpecise details -~~ theoretical mass~~, acutal mass, etc.~~.	+	* 4mL of 133 Au/BSA solution made on 09/11/12 were mixed with 1mL of 50mM Tris buffer at pH 10, yielding a total of 10mM tris buffer in solution. 4mL of 136 Au/BSA solution were mixed with 1mL of 100mM Tris buffer at pH 10, yielding a total of 20mM tris buffer in solution. And 4mL of 138 Au/BSA solution were mixed with 1mL of 500M Tris buffer at pH 10, yielding a total of 100mM tris buffer in solution. All three samples were lightly shaken and let to re-suspend for 30 minutes. Absorbance for the three samples were taken after 30 minutes and after 90 minutes. See [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for results on the absorbance versus wavelength data on each Au/BSA sample. It was concluded that none of the solution were resuspended with the purple fibrous pellet, and the previous experiments cannot be repeated. Tris buffer mixture with Au/BSA resolution remained inconclusive.
-	* Absorbency were measured using UV-vis spectrometer for the sets of Au/BSA samples made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]]. 1mL of each sample were used for measurement. For details of the absorbance, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]].	+
-	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''': show data here too.	+
-	* 4mL of 133 Au/BSA solution made on 09/11/12 were mixed with 1mL of 50mM Tris buffer at pH 10, yielding a total of 10mM tris buffer in solution. 4mL of 136 Au/BSA solution were mixed with 1mL of 100mM Tris buffer at pH 10, yielding a total of 20mM tris buffer in solution. And 4mL of 138 Au/BSA solution were mixed with 1mL of 500M Tris buffer at pH 10, yielding a total of 100mM tris buffer in solution. All three samples were lightly shaken and let to re-suspend for 30 minutes. Absorbance for the three samples were taken after 30 minutes and after 90 minutes. See [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for results.	+
-	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''':show data ~~here too~~. ~~what conclusions can you draw from~~ the ~~data?~~	+

	==Notes==		==Notes==
	* New sets of solutions were taken out of the incubator. Fibers were formed in all samples. It was suspected that the ratios prepared were wrong and all ratios are predicted to be above 133 Au/BSA. Supernatant were clear and fibers were formed closely together as pellet.		* New sets of solutions were taken out of the incubator. Fibers were formed in all samples. It was suspected that the ratios prepared were wrong and all ratios are predicted to be above 133 Au/BSA. Supernatant were clear and fibers were formed closely together as pellet.
-	* Sets of solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced homogeneous solutions at lower ratio and fibers at higher ratios of Au/BSA ~~according~~ to ~~predicted.~~	+	* Sets of solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced homogeneous solutions at lower ratio and fibers at higher ratios of Au/BSA as previous experiments performed by other researchers. It was concluded that the ratios of Au/BSA calculations were correct, and that the procedure were reproducible. For details of the solution, please refer to [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's notebook]] for the appearance of solution for a better understanding of the structural formation of fibers and appearance of pellet and supernatant after incubation.
-	*'''[[User:~~Abigail E. Miller~~\|~~Abigail E. Miller~~]] ~~10:59, 17 September 2012 (EDT)''':be specific. what was predicted? photos~~ of ~~solutions? what ratios produced~~ fibers~~? what produced nothing? what produced homogenous solutions?~~	+
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Abigail E. Miller: /* Procedure */

Abigail E. Miller — Mon, 17 Sep 2012 14:59:41 GMT

Procedure

←Older revision		Revision as of 14:59, 17 September 2012
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	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''': show data here too.		*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''': show data here too.
	* 4mL of 133 Au/BSA solution made on 09/11/12 were mixed with 1mL of 50mM Tris buffer at pH 10, yielding a total of 10mM tris buffer in solution. 4mL of 136 Au/BSA solution were mixed with 1mL of 100mM Tris buffer at pH 10, yielding a total of 20mM tris buffer in solution. And 4mL of 138 Au/BSA solution were mixed with 1mL of 500M Tris buffer at pH 10, yielding a total of 100mM tris buffer in solution. All three samples were lightly shaken and let to re-suspend for 30 minutes. Absorbance for the three samples were taken after 30 minutes and after 90 minutes. See [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for results.		* 4mL of 133 Au/BSA solution made on 09/11/12 were mixed with 1mL of 50mM Tris buffer at pH 10, yielding a total of 10mM tris buffer in solution. 4mL of 136 Au/BSA solution were mixed with 1mL of 100mM Tris buffer at pH 10, yielding a total of 20mM tris buffer in solution. And 4mL of 138 Au/BSA solution were mixed with 1mL of 500M Tris buffer at pH 10, yielding a total of 100mM tris buffer in solution. All three samples were lightly shaken and let to re-suspend for 30 minutes. Absorbance for the three samples were taken after 30 minutes and after 90 minutes. See [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for results.
-	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''':show data here too. conclusions ~~form~~ data?	+	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''':show data here too. what conclusions can you draw from the data?

	==Notes==		==Notes==

Abigail E. Miller: /* Notes */

Abigail E. Miller — Mon, 17 Sep 2012 14:59:04 GMT

Notes

←Older revision		Revision as of 14:59, 17 September 2012
Line 26:		Line 26:
	* New sets of solutions were taken out of the incubator. Fibers were formed in all samples. It was suspected that the ratios prepared were wrong and all ratios are predicted to be above 133 Au/BSA. Supernatant were clear and fibers were formed closely together as pellet.		* New sets of solutions were taken out of the incubator. Fibers were formed in all samples. It was suspected that the ratios prepared were wrong and all ratios are predicted to be above 133 Au/BSA. Supernatant were clear and fibers were formed closely together as pellet.
	* Sets of solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced homogeneous solutions at lower ratio and fibers at higher ratios of Au/BSA according to predicted.		* Sets of solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced homogeneous solutions at lower ratio and fibers at higher ratios of Au/BSA according to predicted.
-		+	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:59, 17 September 2012 (EDT)''':be specific. what was predicted? photos of solutions? what ratios produced fibers? what produced nothing? what produced homogenous solutions?
	<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->		<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
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Abigail E. Miller: /* Procedure */

Abigail E. Miller — Mon, 17 Sep 2012 14:58:03 GMT

Procedure

←Older revision		Revision as of 14:58, 17 September 2012
Line 15:		Line 15:
	==Procedure==		==Procedure==
	* Sets of Au/BSA solutions with different ratios were remade from ratio 80 to ratio 170. For details with the volume, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]]. The sets of solutions were incubated in 85°C for four hours. After four hours of incubation, 1mL of supernatant were measured for absorption activity under UV-vis from 700nm to 200nm. For details of the results, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]].		* Sets of Au/BSA solutions with different ratios were remade from ratio 80 to ratio 170. For details with the volume, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]]. The sets of solutions were incubated in 85°C for four hours. After four hours of incubation, 1mL of supernatant were measured for absorption activity under UV-vis from 700nm to 200nm. For details of the results, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]].
		+	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''':masses and volumes and ratios. can reference the calculations and precise details are in Dhea's notebook.
	* 100mM Tris buffer at pH 10 were diluted to 50mM Tris buffer at pH 10 with distilled water. 1M Tris buffer were made, pH were adjusted to pH 10 with the addition of 1M HCl as stock solution stored in fridge. 500mM Tris buffer at pH 10 were made by diluting from 1M Tris buffer.		* 100mM Tris buffer at pH 10 were diluted to 50mM Tris buffer at pH 10 with distilled water. 1M Tris buffer were made, pH were adjusted to pH 10 with the addition of 1M HCl as stock solution stored in fridge. 500mM Tris buffer at pH 10 were made by diluting from 1M Tris buffer.
		+	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''':masses and volumes and ratios. can reference the calculations and rpecise details - theoretical mass, acutal mass, etc..
	* Absorbency were measured using UV-vis spectrometer for the sets of Au/BSA samples made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]]. 1mL of each sample were used for measurement. For details of the absorbance, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]].		* Absorbency were measured using UV-vis spectrometer for the sets of Au/BSA samples made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]]. 1mL of each sample were used for measurement. For details of the absorbance, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]].
		+	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''': show data here too.
	* 4mL of 133 Au/BSA solution made on 09/11/12 were mixed with 1mL of 50mM Tris buffer at pH 10, yielding a total of 10mM tris buffer in solution. 4mL of 136 Au/BSA solution were mixed with 1mL of 100mM Tris buffer at pH 10, yielding a total of 20mM tris buffer in solution. And 4mL of 138 Au/BSA solution were mixed with 1mL of 500M Tris buffer at pH 10, yielding a total of 100mM tris buffer in solution. All three samples were lightly shaken and let to re-suspend for 30 minutes. Absorbance for the three samples were taken after 30 minutes and after 90 minutes. See [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for results.		* 4mL of 133 Au/BSA solution made on 09/11/12 were mixed with 1mL of 50mM Tris buffer at pH 10, yielding a total of 10mM tris buffer in solution. 4mL of 136 Au/BSA solution were mixed with 1mL of 100mM Tris buffer at pH 10, yielding a total of 20mM tris buffer in solution. And 4mL of 138 Au/BSA solution were mixed with 1mL of 500M Tris buffer at pH 10, yielding a total of 100mM tris buffer in solution. All three samples were lightly shaken and let to re-suspend for 30 minutes. Absorbance for the three samples were taken after 30 minutes and after 90 minutes. See [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for results.
		+	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:58, 17 September 2012 (EDT)''':show data here too. conclusions form data?

	==Notes==		==Notes==

Abigail E. Miller: /* Purpose */

Abigail E. Miller — Mon, 17 Sep 2012 14:55:20 GMT

Purpose

←Older revision		Revision as of 14:55, 17 September 2012
Line 9:		Line 9:
	* To check if solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced fibers		* To check if solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced fibers
	* To mix supernatant of sample with fiber pellet with different concentration of Tris buffer at pH 10 and check re-suspension		* To mix supernatant of sample with fiber pellet with different concentration of Tris buffer at pH 10 and check re-suspension
		+	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:55, 17 September 2012 (EDT)''':I'm confused by this. are you adding tris to the pelletonly, to just the supernatant or to both?
	* Prepare the ratio 80 Au/BSA sample for peak shift testing next week		* Prepare the ratio 80 Au/BSA sample for peak shift testing next week
		+	*'''[[User:Abigail E. Miller\|Abigail E. Miller]] 10:55, 17 September 2012 (EDT)''':explain what hte peak shift experiemnt is.

	==Procedure==		==Procedure==

Keyun Wang at 20:36, 12 September 2012

Keyun Wang — Wed, 12 Sep 2012 20:36:51 GMT

←Older revision		Revision as of 20:36, 12 September 2012
Line 12:		Line 12:

	==Procedure==		==Procedure==
		+	* Sets of Au/BSA solutions with different ratios were remade from ratio 80 to ratio 170. For details with the volume, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]]. The sets of solutions were incubated in 85°C for four hours. After four hours of incubation, 1mL of supernatant were measured for absorption activity under UV-vis from 700nm to 200nm. For details of the results, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]].
		+	* 100mM Tris buffer at pH 10 were diluted to 50mM Tris buffer at pH 10 with distilled water. 1M Tris buffer were made, pH were adjusted to pH 10 with the addition of 1M HCl as stock solution stored in fridge. 500mM Tris buffer at pH 10 were made by diluting from 1M Tris buffer.
		+	* Absorbency were measured using UV-vis spectrometer for the sets of Au/BSA samples made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]]. 1mL of each sample were used for measurement. For details of the absorbance, see [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]].
		+	* 4mL of 133 Au/BSA solution made on 09/11/12 were mixed with 1mL of 50mM Tris buffer at pH 10, yielding a total of 10mM tris buffer in solution. 4mL of 136 Au/BSA solution were mixed with 1mL of 100mM Tris buffer at pH 10, yielding a total of 20mM tris buffer in solution. And 4mL of 138 Au/BSA solution were mixed with 1mL of 500M Tris buffer at pH 10, yielding a total of 100mM tris buffer in solution. All three samples were lightly shaken and let to re-suspend for 30 minutes. Absorbance for the three samples were taken after 30 minutes and after 90 minutes. See [[User:Dhea Patel/Notebook/Experimental Biological Chemistry Notebook/2012/09/12\|Dhea's Notebook]] for results.
		+
		+	==Notes==
		+	* New sets of solutions were taken out of the incubator. Fibers were formed in all samples. It was suspected that the ratios prepared were wrong and all ratios are predicted to be above 133 Au/BSA. Supernatant were clear and fibers were formed closely together as pellet.
		+	* Sets of solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced homogeneous solutions at lower ratio and fibers at higher ratios of Au/BSA according to predicted.

	<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->		<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->

Keyun Wang at 18:40, 12 September 2012

Keyun Wang — Wed, 12 Sep 2012 18:40:23 GMT

←Older revision		Revision as of 18:40, 12 September 2012
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	{\|{{table}} width="800"		{\|{{table}} width="800"
	\|-		\|-
-	\|style="background-color: #EEE"\|[[Image:owwnotebook_icon.png\|128px]]<span style="font-size:22px;"> ~~Project name~~</span>	+	\|style="background-color: #EEE"\|[[Image:owwnotebook_icon.png\|128px]]<span style="font-size:22px;"> Experimental Biological Chemistry I</span>
	\|style="background-color: #F2F2F2" align="center"\|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}\|0\|-11}}\|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}\|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>      </html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}\|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}		\|style="background-color: #F2F2F2" align="center"\|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}\|0\|-11}}\|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}\|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>      </html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}\|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
	\|-		\|-
	\| colspan="2"\|		\| colspan="2"\|
	<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->		<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
-	==~~Entry title~~==	+	==Purpose==
-	* ~~Insert content here...~~	+	* To check if solutions made on [[User:Keyun Wang/Notebook/Experimental Biological Chemistry I/2012/09/11\|2012/09/11]] has produced fibers
		+	* To mix supernatant of sample with fiber pellet with different concentration of Tris buffer at pH 10 and check re-suspension
		+	* Prepare the ratio 80 Au/BSA sample for peak shift testing next week

		+	==Procedure==

	<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->		<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->

Keyun Wang: Autocreate 2012/09/12 Entry for User:Keyun_Wang/Notebook/Experimental_Biological_Chemistry_I

Keyun Wang — Wed, 12 Sep 2012 18:32:51 GMT

Autocreate 2012/09/12 Entry for User:Keyun_Wang/Notebook/Experimental_Biological_Chemistry_I

New page

{|{{table}} width="800"
|-
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>      </html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
|-
| colspan="2"|

==Entry title==
* Insert content here...


|}

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