Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography
Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a po...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
1982 |
|---|
| Reproduktion: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
|---|---|
| Übergeordnetes Werk: |
in: Analytical Biochemistry - Amsterdam : Elsevier, 120(1982), 2, Seite 289-301 |
| Übergeordnetes Werk: |
volume:120 ; year:1982 ; number:2 ; pages:289-301 |
| Links: |
|---|
| Katalog-ID: |
NLEJ183945840 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | NLEJ183945840 | ||
| 003 | DE-627 | ||
| 005 | 20210706215458.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 070506s1982 xx |||||o 00| ||eng c | ||
| 035 | |a (DE-627)NLEJ183945840 | ||
| 035 | |a (DE-599)GBVNLZ183945840 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 245 | 1 | 0 | |a Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography |
| 264 | 1 | |c 1982 | |
| 336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
| 337 | |a nicht spezifiziert |b z |2 rdamedia | ||
| 338 | |a nicht spezifiziert |b zu |2 rdacarrier | ||
| 520 | |a Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. | ||
| 533 | |f Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 | ||
| 700 | 1 | |a Yuan, P.-M. |4 oth | |
| 700 | 1 | |a Pande, H. |4 oth | |
| 700 | 1 | |a Clark, B.R. |4 oth | |
| 700 | 1 | |a Shively, J.E. |4 oth | |
| 773 | 0 | 8 | |i in |t Analytical Biochemistry |d Amsterdam : Elsevier |g 120(1982), 2, Seite 289-301 |w (DE-627)NLEJ17685830X |w (DE-600)1461105-3 |x 0003-2697 |7 nnns |
| 773 | 1 | 8 | |g volume:120 |g year:1982 |g number:2 |g pages:289-301 |
| 856 | 4 | 0 | |u http://dx.doi.org/10.1016/0003-2697(82)90350-5 |
| 912 | |a GBV_USEFLAG_H | ||
| 912 | |a ZDB-1-SDJ | ||
| 912 | |a GBV_NL_ARTICLE | ||
| 951 | |a AR | ||
| 952 | |d 120 |j 1982 |e 2 |h 289-301 | ||
| matchkey_str |
article:00032697:1982----::irsqecaayioppieadrtispeaainfapebrvre |
|---|---|
| hierarchy_sort_str |
1982 |
| publishDate |
1982 |
| allfields |
(DE-627)NLEJ183945840 (DE-599)GBVNLZ183945840 DE-627 ger DE-627 rakwb eng Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography 1982 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Yuan, P.-M. oth Pande, H. oth Clark, B.R. oth Shively, J.E. oth in Analytical Biochemistry Amsterdam : Elsevier 120(1982), 2, Seite 289-301 (DE-627)NLEJ17685830X (DE-600)1461105-3 0003-2697 nnns volume:120 year:1982 number:2 pages:289-301 http://dx.doi.org/10.1016/0003-2697(82)90350-5 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 120 1982 2 289-301 |
| spelling |
(DE-627)NLEJ183945840 (DE-599)GBVNLZ183945840 DE-627 ger DE-627 rakwb eng Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography 1982 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Yuan, P.-M. oth Pande, H. oth Clark, B.R. oth Shively, J.E. oth in Analytical Biochemistry Amsterdam : Elsevier 120(1982), 2, Seite 289-301 (DE-627)NLEJ17685830X (DE-600)1461105-3 0003-2697 nnns volume:120 year:1982 number:2 pages:289-301 http://dx.doi.org/10.1016/0003-2697(82)90350-5 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 120 1982 2 289-301 |
| allfields_unstemmed |
(DE-627)NLEJ183945840 (DE-599)GBVNLZ183945840 DE-627 ger DE-627 rakwb eng Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography 1982 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Yuan, P.-M. oth Pande, H. oth Clark, B.R. oth Shively, J.E. oth in Analytical Biochemistry Amsterdam : Elsevier 120(1982), 2, Seite 289-301 (DE-627)NLEJ17685830X (DE-600)1461105-3 0003-2697 nnns volume:120 year:1982 number:2 pages:289-301 http://dx.doi.org/10.1016/0003-2697(82)90350-5 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 120 1982 2 289-301 |
| allfieldsGer |
(DE-627)NLEJ183945840 (DE-599)GBVNLZ183945840 DE-627 ger DE-627 rakwb eng Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography 1982 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Yuan, P.-M. oth Pande, H. oth Clark, B.R. oth Shively, J.E. oth in Analytical Biochemistry Amsterdam : Elsevier 120(1982), 2, Seite 289-301 (DE-627)NLEJ17685830X (DE-600)1461105-3 0003-2697 nnns volume:120 year:1982 number:2 pages:289-301 http://dx.doi.org/10.1016/0003-2697(82)90350-5 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 120 1982 2 289-301 |
| allfieldsSound |
(DE-627)NLEJ183945840 (DE-599)GBVNLZ183945840 DE-627 ger DE-627 rakwb eng Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography 1982 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Yuan, P.-M. oth Pande, H. oth Clark, B.R. oth Shively, J.E. oth in Analytical Biochemistry Amsterdam : Elsevier 120(1982), 2, Seite 289-301 (DE-627)NLEJ17685830X (DE-600)1461105-3 0003-2697 nnns volume:120 year:1982 number:2 pages:289-301 http://dx.doi.org/10.1016/0003-2697(82)90350-5 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 120 1982 2 289-301 |
| language |
English |
| source |
in Analytical Biochemistry 120(1982), 2, Seite 289-301 volume:120 year:1982 number:2 pages:289-301 |
| sourceStr |
in Analytical Biochemistry 120(1982), 2, Seite 289-301 volume:120 year:1982 number:2 pages:289-301 |
| format_phy_str_mv |
Article |
| institution |
findex.gbv.de |
| isfreeaccess_bool |
false |
| container_title |
Analytical Biochemistry |
| authorswithroles_txt_mv |
Yuan, P.-M. @@oth@@ Pande, H. @@oth@@ Clark, B.R. @@oth@@ Shively, J.E. @@oth@@ |
| publishDateDaySort_date |
1982-01-01T00:00:00Z |
| hierarchy_top_id |
NLEJ17685830X |
| id |
NLEJ183945840 |
| language_de |
englisch |
| fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ183945840</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210706215458.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070506s1982 xx |||||o 00| ||eng c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ183945840</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)GBVNLZ183945840</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1982</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Elsevier Journal Backfiles on ScienceDirect 1907 - 2002</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yuan, P.-M.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Pande, H.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Clark, B.R.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Shively, J.E.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Analytical Biochemistry</subfield><subfield code="d">Amsterdam : Elsevier</subfield><subfield code="g">120(1982), 2, Seite 289-301</subfield><subfield code="w">(DE-627)NLEJ17685830X</subfield><subfield code="w">(DE-600)1461105-3</subfield><subfield code="x">0003-2697</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:120</subfield><subfield code="g">year:1982</subfield><subfield code="g">number:2</subfield><subfield code="g">pages:289-301</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1016/0003-2697(82)90350-5</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_H</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-SDJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">120</subfield><subfield code="j">1982</subfield><subfield code="e">2</subfield><subfield code="h">289-301</subfield></datafield></record></collection>
|
| series2 |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)NLEJ17685830X |
| format |
electronic Article |
| delete_txt_mv |
keep |
| collection |
NL |
| remote_str |
true |
| illustrated |
Not Illustrated |
| issn |
0003-2697 |
| topic_title |
Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography |
| format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
zu |
| author2_variant |
p m y pmy h p hp b c bc j s js |
| hierarchy_parent_title |
Analytical Biochemistry |
| hierarchy_parent_id |
NLEJ17685830X |
| hierarchy_top_title |
Analytical Biochemistry |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)NLEJ17685830X (DE-600)1461105-3 |
| title |
Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography |
| spellingShingle |
Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography |
| ctrlnum |
(DE-627)NLEJ183945840 (DE-599)GBVNLZ183945840 |
| title_full |
Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography |
| journal |
Analytical Biochemistry |
| journalStr |
Analytical Biochemistry |
| lang_code |
eng |
| isOA_bool |
false |
| recordtype |
marc |
| publishDateSort |
1982 |
| contenttype_str_mv |
zzz |
| container_start_page |
289 |
| container_volume |
120 |
| format_se |
Elektronische Aufsätze |
| title_sort |
microsequence analysis of peptides and proteins - i. preparation of samples by reverse-phase liquid chromatography |
| title_auth |
Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography |
| abstract |
Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. |
| abstractGer |
Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. |
| abstract_unstemmed |
Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated. |
| collection_details |
GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE |
| container_issue |
2 |
| title_short |
Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography |
| url |
http://dx.doi.org/10.1016/0003-2697(82)90350-5 |
| remote_bool |
true |
| author2 |
Yuan, P.-M. Pande, H. Clark, B.R. Shively, J.E. |
| author2Str |
Yuan, P.-M. Pande, H. Clark, B.R. Shively, J.E. |
| ppnlink |
NLEJ17685830X |
| mediatype_str_mv |
z |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| author2_role |
oth oth oth oth |
| up_date |
2024-07-05T23:42:08.511Z |
| _version_ |
1803784477485301760 |
| fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ183945840</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210706215458.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070506s1982 xx |||||o 00| ||eng c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ183945840</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)GBVNLZ183945840</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Microsequence analysis of peptides and proteins - I. Preparation of samples by reverse-phase liquid chromatography</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1982</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Reverse-phase supports for the separation of peptides and proteins are compared in two high-performance liquid chromatographic systems. One uses a trifluoroacetic acid-acetonitrile solvent system with a 206-nm detector, and the other uses pyridine-formate or pyridine-acetate and 1-propanol with a postcolumn fluorescence detector. Each system was examined with RP8, RP18, and alkylphenyl supports. In most applications, the trifluoroacetic acid-acetonitrile solvent system used in conjunction with an alkylphenyl column performed best. The use of this system for the preparation of low-microgram amounts of samples for microsequence analysis is illustrated.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Elsevier Journal Backfiles on ScienceDirect 1907 - 2002</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yuan, P.-M.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Pande, H.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Clark, B.R.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Shively, J.E.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Analytical Biochemistry</subfield><subfield code="d">Amsterdam : Elsevier</subfield><subfield code="g">120(1982), 2, Seite 289-301</subfield><subfield code="w">(DE-627)NLEJ17685830X</subfield><subfield code="w">(DE-600)1461105-3</subfield><subfield code="x">0003-2697</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:120</subfield><subfield code="g">year:1982</subfield><subfield code="g">number:2</subfield><subfield code="g">pages:289-301</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1016/0003-2697(82)90350-5</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_H</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-SDJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">120</subfield><subfield code="j">1982</subfield><subfield code="e">2</subfield><subfield code="h">289-301</subfield></datafield></record></collection>
|
| score |
7.401906 |