DEH0008328MA - - Google Patents
Info
- Publication number
- DEH0008328MA DEH0008328MA DEH0008328MA DE H0008328M A DEH0008328M A DE H0008328MA DE H0008328M A DEH0008328M A DE H0008328MA
- Authority
- DE
- Germany
- Prior art keywords
- color
- character
- characters
- brightness
- components
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000003086 colorant Substances 0.000 claims description 34
- 230000000051 modifying Effects 0.000 claims description 25
- 230000005540 biological transmission Effects 0.000 claims description 20
- 239000002131 composite material Substances 0.000 claims description 20
- 230000000875 corresponding Effects 0.000 claims description 19
- 230000000694 effects Effects 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 14
- 230000035945 sensitivity Effects 0.000 claims description 13
- 230000001702 transmitter Effects 0.000 claims description 12
- 230000003321 amplification Effects 0.000 claims description 5
- 238000003199 nucleic acid amplification method Methods 0.000 claims description 5
- 230000002787 reinforcement Effects 0.000 claims description 2
- 235000020127 ayran Nutrition 0.000 claims 1
- 235000019525 fullness Nutrition 0.000 claims 1
- 230000001360 synchronised Effects 0.000 description 13
- 239000000969 carrier Substances 0.000 description 8
- 241001442055 Vipera berus Species 0.000 description 7
- 230000002452 interceptive Effects 0.000 description 5
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- 230000003287 optical Effects 0.000 description 3
- 238000005070 sampling Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 230000002829 reduced Effects 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 230000002238 attenuated Effects 0.000 description 1
- 230000000903 blocking Effects 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- KEBHLNDPKPIPLI-UHFFFAOYSA-N hydron;2-(3H-inden-4-yloxymethyl)morpholine;chloride Chemical compound Cl.C=1C=CC=2C=CCC=2C=1OCC1CNCCO1 KEBHLNDPKPIPLI-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000036961 partial Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 230000001105 regulatory Effects 0.000 description 1
- 230000033764 rhythmic process Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003595 spectral Effects 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- UPKAWFACSJWKND-ZXFFUEEESA-J tetrasodium;(6E)-4-amino-6-[[4-[4-[(2Z)-2-(8-amino-1-oxo-5,7-disulfonatonaphthalen-2-ylidene)hydrazinyl]-3-methoxyphenyl]-2-methoxyphenyl]hydrazinylidene]-5-oxonaphthalene-1,3-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C\1=CC2=C(S([O-])(=O)=O)C=C(S([O-])(=O)=O)C(N)=C2C(=O)C/1=N/NC(C(OC)=C1)=CC=C1C1=CC=C(N\N=C\2C(C3=C(N)C(=CC(=C3C=C/2)S([O-])(=O)=O)S([O-])(=O)=O)=O)C(OC)=C1 UPKAWFACSJWKND-ZXFFUEEESA-J 0.000 description 1
Family
ID=
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