최근 카페에서 쿠폰번호를 받아 시작해본 게임..
MORPG는 처음 해보는데....
시원시원하니 즐겁게 해본것 같다...
흠이라면...인스턴트 던젼을 만들어 하는데....맵 크기가 다소 작은것 같다...
아직 상위 레벨의 맵을 하지 못해서 그런가...다소 짧은 시간의 플레이였다는게..
몬스터들의 AI는 나름 신선 했던것 같다....어떤 것들은 뒤로 돌아서 뒷치기를 하려는..
그런 몬스터도 있었으니...ㅡㅡ;;
단순히 플레이어를 보도 따라오고 몰려다니는 평범한 MMORPG를 해왔던
나로서는 신선한 플레이었다.
'업어온글'에 해당되는 글 32건
- 2009/03/06 요즘 할만한 게임 - C9 - Asteria
- 2009/02/05 세계최초 노트북 전용 모니터 SyncMaster Lapfit(싱크마스터 랩핏) 출시 - Asteria
- 2008/12/12 Adobe Flash Player 9 설치하기 - Asteria
- 2008/11/18 Information of E-coli Genotype - Asteria
- 2008/08/10 Ubuntu nabi 설치 및 설정하기 - Asteria
요즘 할만한 게임 - C9
세계최초 노트북 전용 모니터 SyncMaster Lapfit(싱크마스터 랩핏) 출시
Adobe Flash Player 9 설치하기
-이 포스팅은 저의 Textcube 블로그에서 그대로 복사하여 살짝 수정한 내용입니다-
안녕하세요. 다사홈 운영자 D.Kim입니다.
최근 자유게시판 등 거의 모든 게시판에서 첨부가 안된다고 호소하는 경우가 있으셔서 이런 공지를 올립니다. 아래에 해결방법이 있으니 참고 바랍니다.
이번 문제는 Adobe Flash Player 9 에서 Adobe Flash Player 10으로 업데이트 되면서 발생한 문제입니다. 이에 대한 해결방법은 Adobe Flash Player 9로 다운그레이드 하는 것이며, 파일과 방법은 다음과 같습니다.
1. 아래의 파일을 다운 받아 Adobe Flash Player 를 제거합니다.
2. 아래의 파일을 다운 받아 Adobe Flash Player9를 설치합니다.
3.브라우저를 다 끄시고 다시 켜보시면 됩니다.
아마 Naver blog, Textcube(저장완료 1회 버그있음) 에서 효과를 보실수가 있습니다.
*파이어폭스를 사용시 다사홈에서는 이렇게 패치해도 해결이 안되는 경우가 있습니다.
그때에는 이렇게해주시고 나타난 새탭에서 파일첨부를 사용해주시면 99.9% 됩니다.
물론 이 방법은 Adobe Flash Player10에서도 동일합니다.
Information of E-coli Genotype
출처 : openwetware
Nomenclature & Abbreviations
A listed gene name means that gene carries a loss of function mutation, a Δ preceding a gene name means the gene is deleted. If a gene is not listed, it is not known to be mutated. Prophages present in wt K-12 strains (F, λ, e14, rac) are listed only if absent. E. coli B strains are naturally lon- and dcm-.
- F- = Does not carry the F plasmid
- F+ = Carries the F plasmid. The cell is able to mate with F- through conjugation.
- F'[ ] = Carries an F plasmid that has host chromosomal genes on it from a previous recombination event. This cell can also mate with F- through conjugation. Chromosomal genes carried in the F plasmid are listed in brackets.
- rB/K+/- = The (B/K) defines the strain lineage. The +/- indicates whether the strain has or hasn't got the restriction system.
- mB/K+/- = The (B/K) defines the strain lineage. The +/- indicates whether the strain has or hasn't got the modification (methylation) system.
- hsdS = Both restriction and methylation of certain sequences is deleted from the strain. If you transform DNA from such a strain into a wild type strain, it will be degraded.
- hsdR = For efficient transformation of cloned unmethylated DNA from PCR amplifications
- INV( ) = chromosomal inversion between locations indicated
- ahpC = mutation to alkyl hydroperoxide reductase conferring disulfide reductase activity
- ara-14 = cannot metabolize arabinose
- araD = mutation in L-ribulose-phosphate 4-epimerase blocks arabinose metabolism
- cycA = mutation in alanine transporter; cannot use alanine as a carbon source
- dapD = mutation in succinyl diaminopimelate aminotransferase leads to succinate or (lysine + methionine) requirement
- Δ( ) = chromosomal deletion of genes between the listed genes (may include unlisted genes!)
- dam = adenine methylation at GATC sequences abolished; high recombination efficiency; DNA repair turned on
- dcm = cytosine methylation at second C of CCWGG sites abolished
- deoR = regulatory gene that allows constitutive expression of deoxyribose synthesis genes; permits uptake of large plasmids. See Hanahan D, US Patent 4,851,348. ***This has been called into question, as the DH10B genome sequence revealed that it is deoR+. See Durfee08, PMID 18245285.
- dnaJ = one of the chaparonins inactivated; stabilizes some mutant proteins
- dut1 = dUTPase activity abolished, leading to increased dUTP concentrations, allowing uracil instead of thymine incorporation in DNA. Stable U incorporation requires ung gene mutation as well.
- endA1 = For cleaner preparations of DNA and better results in downstream applications due to the elimination of non-specific digestion by Endonuclease I
- (e14) = excisable prophage like element containing mcrA gene; present in K-12 but missing in many other strains
- galE = mutations are associated with high competence, increased resistance to phage P1 infection, and 2-deoxygalactose resistance. galE mutations block the production of UDP-galactose, resulting in truncation of LPS glycans to the minimal, "inner core". The exceptional competence of DH10B/TOP10 is thought to be a result of a reduced interference from LPS in the binding and/or uptake of transforming DNA. galE15 is a point mutation resulting in a Ser123 -> Phe conversion near the enzyme's active site. See van Die, et al. PMID 6373734, Hanahan, et al. PMID 1943786, and EcoSal ISBN 1555811647. --Dcekiert 16:56, 23 January 2008 (CST)
- galk = mutants cannot metabolize galactose and are resistant to 2-deoxygalactose. galK16 is an IS2 insertion ~170bp downstream of the galK start codon. See EcoSal ISBN 1555811647. --Dcekiert 16:56, 23 January 2008 (CST)
- galU = mutants cannot metabolize galactose
- gor = mutation in glutathione reductase; enhances disulphide bond formation
- glnV = suppression of amber (UAG) stop codons by insertion of glutamine; required for some phage growth
- gyrA96 = mutation in DNA gyrase; conveys nalidixic acid resistance
- gyrA462 = mutation in DNA gyrase; conveys resistance to ccdB colicin gene product
- hflA150 = protease mutation stabilizing phage cII protein; high frequency of lysogenization by λ
- Δ(lac)X74 = Deletion of the entire lac operon as well as some flanking DNA.
- lacIq or lacIQ = overproduction of the lac repressor protein; -35 site in promoter upstream of lacI is mutated from GCGCAA to GTGCAA
- lacIQ1 = overproduction of the lac repressor protein; contains a 15 bp deletion to create optimal -35 site in promoter upstream of lacI
- lacY = deficient in lactose transport; deletion of lactose permease (M protein)
- lacZΔM15 = partial deletion of the lacZ gene that allows α complementation of the β-galactosidase gene; required for blue/white selection on XGal plates. Deletes the amino portion of lacZ (aa 11-41).
- leuB = requires leucine
- Δlon = deletion of the lon protease
- malA = cannot metabolize maltose
- mcrA = Mutation eliminating restriction of DNA methylated at the sequence CmCGG (possibly mCG). Carried on the e14 prophage (q.v.)
- mcrB = Mutation eliminating restriction of DNA methylated at the sequence RmC
- metB = requires methionine
- metC = requires methionine
- mrr = Mutation eliminating restriction of DNA methylated at the sequence CmAG or GmAC
- mtlA = cannot metabilize mannitol
- (Mu) = Mu prophage present. Muδ means the phage is defective.
- mutS - mutation inhibits DNA repair of mismatches in unmethylated newly synthesized strands
- nupG = same as deoR
- ompT = mutation in outer membrane protein protease VII, reducing proteolysis of expressed proteins
- (P1) = Cell carries a P1 prophage. Cells express the P1 restriction system.
- (P2) = Cell carries a P2 prophage. Allows selection against Red+ Gam+ λ
- (φ80) = Cell carries the lambdoid prophage φ80. A defective version of this phage carrying lacZM15 deletion (as well as wild-type lacI, lacYA, and flanking sequences) is present in some strains. The φ80 attachment site is just adjacent to tonB.
- pLysS = contains pLysS plasmid carrying chloramphenicol resistance and phage T7 lysozyme, effective at attenuating activity of T7 RNA polymerase, for better inhibition of expression under non-induced conditions. The sequence can be found here.
- proA/B = requires proline
- recA1 = For reduced occurrence of unwanted recombination in cloned DNA; cells UV sensitive, deficient in DNA repair
- recA13 = as for recA1, but inserts less stable.
- recBCD = Exonuclease V; mutation in RecB or RecC reduces general recombination by a factor of 100; impaired DNA repair; UV sensitive, easier propagation of inverted repeats
- recJ Exonuclease involved in alternate recombination
- relA = relaxed phenotype; permits RNA synthesis in absence of protein synthesis
- rha = blocked rhamose metabolism
- rnc = encodes RnaseIII (rnc-14 is a common null mutant)
- rne = encodes RnaseE (rne-3071 is a common temperature sensitive mutant)
- rpsL = mutation in ribosomal protein S12 conveying streptomycin resistance; also called strA
- sbcBC = ExoI activity abolished; usually present in recBC strains; recombination proficient, stable inverted repeats
- sr1 = cannot metabolize sorbitol
- supE = glnV
- supF = tyrT
- thi = requires thiamine
- thyA = requires thymidine
- Tn10 = transposon normally carrying Tetracycline resistance
- Tn5 = transposon normally carrying Kanamycin resistance
- tonA = Mutation in outer membrane protein conveying resistance to phage T1 and phage T5
- traD = Mutation eliminating transfer factor; prevents transfer of F plasmid
- trxB = mutation in thioredoxin reductase; enhances disulphide bond formation in the cytoplasm
- tsx = outer membrane protein mutation conveying resistance to phage T6 and colicin K
- tryT = suppression of amber (UAG) stop codons by insertion of tyrosine; needed for some phage infection such as λgt11.
- ung1 = allows uracil to exist in plasmid DNA
- xyl-5 = blocked xylose metabolism
- SmR = Streptomycin resistance
Ubuntu nabi 설치 및 설정하기
개인적으로 Ubuntu 활용에 사용하기 위해 -_- | +_+ | -ㅁ- | -ㅂ- | -ㅅ- | -ㅛ- | ( -_-) - ?님 블로그에서 퍼왔습니다.
우분투 설치하면 기본으로 깔려있는 scim이라는 다국어 지원 입력기가 있는데..
이녀석이 심심하면 죽거나;; 잘 되다가 갑자기 안되거나 하는 일이 있으니 답답하기 그지 없어서-_-;;
scim을 기본으로 쓰고 있지만 그걸 전통(!)의 한글 입력기인 nabi로 변경했음..
일단 nabi 설치..
기본 입력기 설정 변경 방법은 터미널 하나 띄우고
#sudo apt-get install nabi
설치 끗…
scim에서 nabi로 설정 변경하기
#sudo im-switch -c
하면 패스워드 넣고 입력기 리스트가 몇개가 나오는데..
나오는 목록 중에 nabi를 찾아서 번호 입력후 엔터..
그리고 리붓 아니면 ctrl+alt+backspace로 X windows만 다시 실행시키면
기본으로 nabi가 실행되어있음..
변경 끗…
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