Suche >
4\\\'-Nitrobiphenyl-3-carbonsäure
Drucken
Sie suchten nach:
130 189 results were found
4\\\'-Nitrobiphenyl-3-carbonsäure
Artikel-Nr:
(APOSOR27103-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR27103-250MG
Lokale Artikelnummer::
APOSOR27103-250MG
Beschreibung:
Ethyl 2-chloro-3-cyano-6-methylisonicotinate
VE:
1 * 250 mg
Artikel-Nr:
(APOSOR955773-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR955773-5G
Lokale Artikelnummer::
APOSOR955773-5G
Beschreibung:
4-Chloro-2-methyl-benzoic acid methyl ester 98%
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-12345R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-A488
Lokale Artikelnummer::
BOSSBS-12345R-A488
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12345R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-A647
Lokale Artikelnummer::
BOSSBS-12345R-A647
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12345R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12345R-A555
Lokale Artikelnummer::
BOSSBS-12345R-A555
Beschreibung:
HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR32187-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR32187-1G
Lokale Artikelnummer::
APOSOR32187-1G
Beschreibung:
5-(3-Chlorophenoxy)-1,3-dimethyl-1H-pyrazole-4-carbaldehyde 95%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
[4-[(Dimethylamino)methyl]phenyl]boronic acid 97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
6,7-Dimethoxy-1,2,3,4-tetrahydroisochinolin Hydrochlorid 97%
Artikel-Nr:
(BLDPBD168824-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD168824-10G
Lokale Artikelnummer::
BLDPBD168824-10G
Beschreibung:
2-Brom-5-fluorisonicotinsäure 97%
VE:
1 * 10 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Boc-trans-4-amino-L-proline methyl ester hydrochloride salt
Artikel-Nr:
(BLDPBD53719-500G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD53719-500G
Lokale Artikelnummer::
BLDPBD53719-500G
Beschreibung:
1,3:2,4-Bis-O-(3,4-dimethylbenzylidene)-D-sorbitol 97%
VE:
1 * 500 g
Artikel-Nr:
(BOSSBS-12946R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12946R-A488
Lokale Artikelnummer::
BOSSBS-12946R-A488
Beschreibung:
CRP2 is a 193 amino acid nuclear protein that belongs to the CRP family of LIM domain proteins. Highly expressed in smooth muscle of aorta, CRP2 is thought to have a role in embryonic vascular system development and is downregulated following cell injury or PDGF-B exposure. CRP2 contains two LIM zinc-binding domains and is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12946R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12946R-A350
Lokale Artikelnummer::
BOSSBS-12946R-A350
Beschreibung:
CRP2 is a 193 amino acid nuclear protein that belongs to the CRP family of LIM domain proteins. Highly expressed in smooth muscle of aorta, CRP2 is thought to have a role in embryonic vascular system development and is downregulated following cell injury or PDGF-B exposure. CRP2 contains two LIM zinc-binding domains and is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12163R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12163R-A350
Lokale Artikelnummer::
BOSSBS-12163R-A350
Beschreibung:
CAPS2 is a 557 amino acid calcium-binding protein that is abundantly expressed, with highest expression found in placenta, testis, colon, lung and brain. CAPS2 contains three EF-hand domains and exists as three alternatively spliced isoforms. Suggested to play a role in large dense-core vesicle (LDCV) exocytosis, CAPS2 is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12163R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12163R-A750
Lokale Artikelnummer::
BOSSBS-12163R-A750
Beschreibung:
CAPS2 is a 557 amino acid calcium-binding protein that is abundantly expressed, with highest expression found in placenta, testis, colon, lung and brain. CAPS2 contains three EF-hand domains and exists as three alternatively spliced isoforms. Suggested to play a role in large dense-core vesicle (LDCV) exocytosis, CAPS2 is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12946R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12946R-A750
Lokale Artikelnummer::
BOSSBS-12946R-A750
Beschreibung:
CRP2 is a 193 amino acid nuclear protein that belongs to the CRP family of LIM domain proteins. Highly expressed in smooth muscle of aorta, CRP2 is thought to have a role in embryonic vascular system development and is downregulated following cell injury or PDGF-B exposure. CRP2 contains two LIM zinc-binding domains and is encoded by a gene that maps to human chromosome 12, which encodes over 1100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Preis auf Anfrage
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
