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KAS et al.

Tuesday, October 12, 2010. Thursday, July 29, 2010. After we analyzed the sequencing results, actually there were some problems. Basically we manage to get the correct insert (KAS II) into pQE30. The problems also the same as KAS I, but, instead of missing one nucleotide, it happen to be an extra nucleotide at the primer. so, for confirmation, we decided to send for re-sequencing again and compare with other clones. More progress will be updated soon. Friday, July 23, 2010. Only KAS III gave negative res...

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KAS et al. | aboutkas.blogspot.com Reviews
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Tuesday, October 12, 2010. Thursday, July 29, 2010. After we analyzed the sequencing results, actually there were some problems. Basically we manage to get the correct insert (KAS II) into pQE30. The problems also the same as KAS I, but, instead of missing one nucleotide, it happen to be an extra nucleotide at the primer. so, for confirmation, we decided to send for re-sequencing again and compare with other clones. More progress will be updated soon. Friday, July 23, 2010. Only KAS III gave negative res...
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1 kas et al
2 beta ketoacyl acp synthase
3 progress update oct
4 kas i
5 hani
6 posted by
7 hani kila
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9 email this
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kas et al,beta ketoacyl acp synthase,progress update oct,kas i,hani,posted by,hani kila,no comments,email this,blogthis,share to twitter,share to facebook,share to pinterest,progress report 2,kas ii,kas iii,that's all,hadi /hani,hadi,1 comment,thank you
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KAS et al. | aboutkas.blogspot.com Reviews

https://aboutkas.blogspot.com

Tuesday, October 12, 2010. Thursday, July 29, 2010. After we analyzed the sequencing results, actually there were some problems. Basically we manage to get the correct insert (KAS II) into pQE30. The problems also the same as KAS I, but, instead of missing one nucleotide, it happen to be an extra nucleotide at the primer. so, for confirmation, we decided to send for re-sequencing again and compare with other clones. More progress will be updated soon. Friday, July 23, 2010. Only KAS III gave negative res...

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aboutkas.blogspot.com aboutkas.blogspot.com
1

KAS et al.: July 2010

http://www.aboutkas.blogspot.com/2010_07_01_archive.html

Thursday, July 29, 2010. After we analyzed the sequencing results, actually there were some problems. Basically we manage to get the correct insert (KAS II) into pQE30. The problems also the same as KAS I, but, instead of missing one nucleotide, it happen to be an extra nucleotide at the primer. so, for confirmation, we decided to send for re-sequencing again and compare with other clones. More progress will be updated soon. Friday, July 23, 2010. Out of KAS I and KAS II, both samples gave positive result.

2

KAS et al.: progress report 2

http://www.aboutkas.blogspot.com/2010/07/progress-report-2.html

Thursday, July 29, 2010. After we analyzed the sequencing results, actually there were some problems. Basically we manage to get the correct insert (KAS II) into pQE30. The problems also the same as KAS I, but, instead of missing one nucleotide, it happen to be an extra nucleotide at the primer. so, for confirmation, we decided to send for re-sequencing again and compare with other clones. More progress will be updated soon. August 12, 2010 at 6:56 AM. Subscribe to: Post Comments (Atom).

3

KAS et al.: October 2010

http://www.aboutkas.blogspot.com/2010_10_01_archive.html

Tuesday, October 12, 2010. Subscribe to: Posts (Atom). Picture Window template. Powered by Blogger.

4

KAS et al.: progress updated!

http://www.aboutkas.blogspot.com/2010/07/progress-updated.html

Friday, July 23, 2010. Last monday, we sent our plasmid extraction samples (pQE30 KAS in E.coli JM109) for sequencing. Out of KAS I and KAS II, both samples gave positive result. When we have confirm the sequencing result, we will proceed with transformation of pQE30 KAS into E.coli M15 and protein expression. We try to express pQE30 KAS using two different hosts. PQE30 KAS in E.coli JM109, and also pQE30 KAS in E.coli M15. Subscribe to: Post Comments (Atom).

5

KAS et al.: progress update (Oct)

http://www.aboutkas.blogspot.com/2010/10/progress-update-oct.html

Tuesday, October 12, 2010. Subscribe to: Post Comments (Atom). Picture Window template. Powered by Blogger.

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adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: Insoluble protein?!

http://adrian-protein.blogspot.com/2010/08/insoluble-protein.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Wednesday, August 18, 2010. According to SDS P.A.G.E for solubility which I did on 18 AUG, the result doesn't looks good. Maybe it is better to subclone the stored plasmid to Rosetta-gami2 (DE3) and BL21 (DE3) , BL21 (DE3)/pLySs? At the same time, design primer and clone into pCold and pMAL.

adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: August

http://adrian-protein.blogspot.com/2010/08/august.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Monday, August 16, 2010. Last 2 weeks screening for the culture of RG2 pET32 phaCcs between 2 culture from glycerol stock. As a result, one of the bacteria was contamination, didn't express protein phaC and didnt contain the correct plasmids. 17 AUG 2010 (Done). 1 Purification by TALON.

adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: The definition of biodegradability

http://adrian-protein.blogspot.com/2010/12/definition-of-biodegradability.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Wednesday, December 22, 2010. The definition of biodegradability. Towards Common Ground –. Meeting Summary of the International Workshop on Biodegradability,. Annapolis, MD, USA, 1992. Such as composting, sewage treatment, denitrification, or anaerobic sludge treatment. Stuck @ dec 2010.

adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: Crystallization tutorial

http://adrian-protein.blogspot.com/2014/06/crystallization-tutorial.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Wednesday, June 4, 2014. This is a very simple tutorial about protein crystallization:. Http:/ xray.bmc.uu.se/ terese/tutorials.html. Bergfors, T., Editor. Protein Crystallization: Second Edition. 2009. International. University Line, La Jolla, California, 500 pp. KAS project by hani hadi.

adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: December 2010

http://adrian-protein.blogspot.com/2010_12_01_archive.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Wednesday, December 22, 2010. The definition of biodegradability. Towards Common Ground –. Meeting Summary of the International Workshop on Biodegradability,. Annapolis, MD, USA, 1992. Such as composting, sewage treatment, denitrification, or anaerobic sludge treatment. Stuck @ dec 2010.

adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: August 2010

http://adrian-protein.blogspot.com/2010_08_01_archive.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Sunday, August 22, 2010. This week will be a busy week starting from tomorrow. Maybe should say it is a busy month too. I do not want to waste my time anymore. So let's get to work. An amount of bacterial hosts and expression vectors appearing in my minds now. The NEB express - ER2523. As a ...

adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: Stuck @ dec 2010

http://adrian-protein.blogspot.com/2010/12/stuck-dec-2010.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Wednesday, December 8, 2010. Stuck @ dec 2010. E coli Rosettagami2(DE3) with pET32 harbouring pha. Problem 1: Expression level of PhaC is very low compare to previous batches. Less than 10% , will be very difficult to be purified). Problem 2: Almost 100% of the expressed PhaC is insoluble.

adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: July 2010

http://adrian-protein.blogspot.com/2010_07_01_archive.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Friday, July 30, 2010. Was trying to produce more protein from the 1.6L induced bacterial cultures. Purified with Affinity chromatography successfully. (Although lost an amount of protein due to my mistakes). Concentrated it with a protein concentrator since it has been diluted. The culture ...

adrian-protein.blogspot.com adrian-protein.blogspot.com

Dimension: JUNE-JULY

http://adrian-protein.blogspot.com/2010/07/june-july.html

The X-ray study of proteins is sometimes regarded as an abstruse subject comprehensible only to specialists, but the basic ideas underlying our work are so simple that some physicists find them boring. (Perutz 1992). Friday, July 30, 2010. Was trying to produce more protein from the 1.6L induced bacterial cultures. Purified with Affinity chromatography successfully. (Although lost an amount of protein due to my mistakes). Concentrated it with a protein concentrator since it has been diluted.

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KAS et al.

Tuesday, October 12, 2010. Thursday, July 29, 2010. After we analyzed the sequencing results, actually there were some problems. Basically we manage to get the correct insert (KAS II) into pQE30. The problems also the same as KAS I, but, instead of missing one nucleotide, it happen to be an extra nucleotide at the primer. so, for confirmation, we decided to send for re-sequencing again and compare with other clones. More progress will be updated soon. Friday, July 23, 2010. Only KAS III gave negative res...

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