Methyl-6-aminopyrazine-2-carboxylate
Artikel-Nr:
(APOSPC103136-50MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC103136-50MG
Lokale Artikelnummer::
APOSPC103136-50MG
Beschreibung:
6-Bromo-N-(2,4-difluorobenzyl)-4-((2,4-dimethoxybenzyl)amino)-1-((3,4-dimethoxybenzyl)oxy)-2-oxo-1,2-dihydro-1,8-naphthyridine-3-car boxamide 50mg pack 1 * 50 mg
VE:
1 * 50 mg
New Product
Artikel-Nr:
(APOSOR945146-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR945146-5G
Lokale Artikelnummer::
APOSOR945146-5G
Beschreibung:
(2,4-Dimethoxybenzyl)methylamine 97%
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-11769R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11769R-A488
Lokale Artikelnummer::
BOSSBS-11769R-A488
Beschreibung:
The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,4-Dimethoxybenzylalkohol
Artikel-Nr:
(MSPPSTOCK7S-17066)
Lieferant:
MARKET SOURCE PART PROCESS
Hersteller-Artikelnummer::
STOCK7S-17066
Lokale Artikelnummer::
MSPPSTOCK7S-17066
Beschreibung:
3-(3.4-DIMETHOXYPHENYL)-7-METHYLPYRAZOLO 1 * 50 mg
VE:
1 * 50 mg
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Artikel-Nr:
(APOSPC105083-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC105083-25G
Lokale Artikelnummer::
APOSPC105083-25G
Beschreibung:
1-Cyclopropyl-6-Fluoro-7-((4As,7As)-Hexahydro-1H-Pyrrolo[3,4-B]Pyridin-6(2H)-Yl)-8-Methoxy-4-Oxo-1,4-Dihydroquinoline-3-Carboxylic A cid 25g pack 1 * 25 g
VE:
1 * 25 g
New Product
Artikel-Nr:
(BOSSBS-11769R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11769R-A350
Lokale Artikelnummer::
BOSSBS-11769R-A350
Beschreibung:
The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11769R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11769R-A555
Lokale Artikelnummer::
BOSSBS-11769R-A555
Beschreibung:
The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11769R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11769R-FITC
Lokale Artikelnummer::
BOSSBS-11769R-FITC
Beschreibung:
The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR89540-25MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR89540-25MG
Lokale Artikelnummer::
APOSOR89540-25MG
Beschreibung:
4-(4-(8-Oxa-3-azabicyclo[3.2.1]octan-3-yl)-1-(1,4-dioxaspiro[4.5]decan-8-yl)-1H-pyrazolo[3,4-d]pyrimidin-6-yl)aniline 25mg pack 1 * 25 mg
VE:
1 * 25 mg
New Product
Artikel-Nr:
(MAYBJFD02889.1)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
JFD02889.1
Lokale Artikelnummer::
MAYBJFD02889.1
Beschreibung:
3-(3,4-dimethoxyphenyl)acrylic acid TECH 1 * 1 g
VE:
1 * 1 g
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Artikel-Nr:
(MAYBBTB08729.1)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
BTB08729.1
Lokale Artikelnummer::
MAYBBTB08729.1
Beschreibung:
2-[(3,4-dimethoxyphenyl)thio]acetic acid 1 * 1 g
VE:
1 * 1 g
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Artikel-Nr:
(MAYBBTB09912.10)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
BTB09912.10
Lokale Artikelnummer::
MAYBBTB09912.10
Beschreibung:
(2-chloro-3,4-dimethoxyphenyl)methanol 9 1 * 10 g
VE:
1 * 10 g
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Artikel-Nr:
(BOSSBS-11769R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11769R-A647
Lokale Artikelnummer::
BOSSBS-11769R-A647
Beschreibung:
The majority of mitochondrial-directed proteins are encoded by the nuclear genome and are transported to the mitochondria via regulated processes involving the mitochondrial Tom and Tim proteins (1). The mitochondrial Tim protein family is comprised of a large group of evolutionarily conserved proteins that are found in most eukaryotes (1,2). Import of nuclear-encoded precursor proteins into and across the mitochondrial inner membrane is mediated by two distinct complexes, the Tim23 complex and the Tim22 complex, which differ in their substrate specificity (1). Defects in Tim proteins are implicated in several neuro-degenerative diseases, suggesting important roles for Tim proteins in development and health (3,4). Tim8A and Tim8B, which map to human chromosomes Xq22.1 and 11q23.1-q23.2, respectively, are conserved proteins of the mitochondrial intermembrane space, which are organized in hetero-oligomeric complex with Tim13 (5,6,7). Tim8A is highly expressed in fetal and adult brain (5). Tim8A is mutated in deafness dystonia syndrome, a novel type of disease that causes severe neurological defects, thought to be caused by a defective mitochondrial protein transport system (5,8).
VE:
1 * 100 µl
Artikel-Nr:
(BIOT7K-009.5)
Lieferant:
BIONET RESEARCH
Hersteller-Artikelnummer::
7K-009.5
Lokale Artikelnummer::
BIOT7K-009.5
Beschreibung:
2-cyano(3,4-dimethoxyphenyl)methyl-6-flu 1 * 5 g
VE:
1 * 5 g
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Artikel-Nr:
(BIOT1G-004.1)
Lieferant:
BIONET RESEARCH
Hersteller-Artikelnummer::
1G-004.1
Lokale Artikelnummer::
BIOT1G-004.1
Beschreibung:
4-(3,4-dimethoxyphenyl)-3-methyl-1H-pyra 1 * 1 g
VE:
1 * 1 g
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