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1,2-Phenylendiisothiocyanat
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1,2-Phenylendiisothiocyanat
Artikel-Nr:
(SIAL410829-25ML)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
410829-25ML
Lokale Artikelnummer::
SIAL410829-25ML
Beschreibung:
9,10-Epoxy-1-decen, Sigma-Aldrich®
VE:
1 * 25 mL
Artikel-Nr:
(CPSD8560409)
Lieferant:
CAPITAL SAFETY
Hersteller-Artikelnummer::
8560409
Lokale Artikelnummer::
CPSD8560409
Beschreibung:
This pole hoist attaches to a carabiner on the universal bracket to a suitable anchor point, allowing to work in any direction from any angle.
VE:
1 * 1 ST
Artikel-Nr:
(MOLEM63590011)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M63590011
Lokale Artikelnummer::
MOLEM63590011
Beschreibung:
2-Aminopyrimidin
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(MOLE34778741-500G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
34778741-500G
Lokale Artikelnummer::
MOLE34778741-500G
Beschreibung:
Citrazinsäure
VE:
1 * 500 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-11604R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11604R-A488
Lokale Artikelnummer::
BOSSBS-11604R-A488
Beschreibung:
Na+/Cl- dependent neurotransmitter transporters are a superfamily of transmembrane proteins that contain 12 membrane spanning regions (1). Specifically, the highly hydrophobic Na+/Cl- dependent glycine transporters (GlyT) are crucial for the termination of neurotransmission at glycinergic synapses (2,3). Two different GlyT genes encode GlyT2 and GlyT1, which exists as two isoforms produced by alternative splicing of the same gene located on human chromosome 1p31.3 (3,4). The GlyT1 gene may be an early marker of neural development and encodes glia-specific transporter proteins (3). Although GlyT1 and GlyT2 are both expressed in the brain and spinal cord, each shows a unique pattern of expression (3,5,6). GlyT1 is found only in the white matter of the CNS, whereas GlyT2 is found in the gray matter of the CNS as well as in macrophages and mast cells in peripheral tissues (3,5). The anatomic distribution of GlyT2 mRNA suggests that glycine may act as a supraspinal neurotransmitter and may function as a chemical messenger outside the CNS (5).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11604R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11604R-FITC
Lokale Artikelnummer::
BOSSBS-11604R-FITC
Beschreibung:
Na+/Cl- dependent neurotransmitter transporters are a superfamily of transmembrane proteins that contain 12 membrane spanning regions (1). Specifically, the highly hydrophobic Na+/Cl- dependent glycine transporters (GlyT) are crucial for the termination of neurotransmission at glycinergic synapses (2,3). Two different GlyT genes encode GlyT2 and GlyT1, which exists as two isoforms produced by alternative splicing of the same gene located on human chromosome 1p31.3 (3,4). The GlyT1 gene may be an early marker of neural development and encodes glia-specific transporter proteins (3). Although GlyT1 and GlyT2 are both expressed in the brain and spinal cord, each shows a unique pattern of expression (3,5,6). GlyT1 is found only in the white matter of the CNS, whereas GlyT2 is found in the gray matter of the CNS as well as in macrophages and mast cells in peripheral tissues (3,5). The anatomic distribution of GlyT2 mRNA suggests that glycine may act as a supraspinal neurotransmitter and may function as a chemical messenger outside the CNS (5).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11604R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11604R-A647
Lokale Artikelnummer::
BOSSBS-11604R-A647
Beschreibung:
Na+/Cl- dependent neurotransmitter transporters are a superfamily of transmembrane proteins that contain 12 membrane spanning regions (1). Specifically, the highly hydrophobic Na+/Cl- dependent glycine transporters (GlyT) are crucial for the termination of neurotransmission at glycinergic synapses (2,3). Two different GlyT genes encode GlyT2 and GlyT1, which exists as two isoforms produced by alternative splicing of the same gene located on human chromosome 1p31.3 (3,4). The GlyT1 gene may be an early marker of neural development and encodes glia-specific transporter proteins (3). Although GlyT1 and GlyT2 are both expressed in the brain and spinal cord, each shows a unique pattern of expression (3,5,6). GlyT1 is found only in the white matter of the CNS, whereas GlyT2 is found in the gray matter of the CNS as well as in macrophages and mast cells in peripheral tissues (3,5). The anatomic distribution of GlyT2 mRNA suggests that glycine may act as a supraspinal neurotransmitter and may function as a chemical messenger outside the CNS (5).
VE:
1 * 100 µl
Lieferant:
IKA
Beschreibung:
ICC Kompakt-Einhängethermostate ermöglichen die flexible Kopplung an Wasserbäder unterschiedlicher Volumina. Sie sind für das Temperieren von Flüssigkeiten bis zu Temperaturen von 150 °C ausgelegt. Der praktische Tragegriff und das kompakte Design ermöglichen einen einfachen Transport sowie eine komfortable Nutzung. Eine wirtschaftliche und attraktive Lösung für Basisanwendungen wie das Temperieren von Proben und das Erwärmen von Glaswaren.
Artikel-Nr:
(EHERC15975000)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C15975000
Lokale Artikelnummer::
EHERC15975000
Beschreibung:
Pentamethylbenzol
VE:
1 * 0,5 g
Artikel-Nr:
(MAYBCC00612.250)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
CC00612.250
Lokale Artikelnummer::
MAYBCC00612.250
Beschreibung:
3,5-Dimethyl-4-isoxazolboronsäure
VE:
1 * 250 mg
This is a MarketSource item. Additional charges may apply
Lieferant:
Sigma-Aldrich
Beschreibung:
Propiononitril, Sigma-Aldrich®
Lieferant:
FLUOROCHEM
Beschreibung:
3,4-Dimethylbenzotrifluorid
Artikel-Nr:
(BOSSBS-11512R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11512R-A750
Lokale Artikelnummer::
BOSSBS-11512R-A750
Beschreibung:
Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterised by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11843R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11843R-A555
Lokale Artikelnummer::
BOSSBS-11843R-A555
Beschreibung:
Growth/differentiation factors (GDFs) are members of the TGF superfamily (1,2). Members of the TGF superfamily are involved in embryonic development and adult tissue homeostasis (1). GDF-1 expression is almost exclusively restricted to the central nervous system and mediates cell differentiation events during embryonic development (3). Neither GDF-3 (Vgr-2) nor GDF-9 contains the conserved cysteine residue which is found in most other TGF superfamily members. GDF-3 is detectable in bone marrow, spleen, thymus and adipose tissue, whereas GDF-9 has only been detected in ovary (4). GDF-5 (also designated CDMP-1) has been shown to induce activation of plasminogen activator, thereby inducing angiogenesis. It is predominantly expressed in long bones during fetal embryonic development and is involved in bone formation. (5). GDF-5 mutations have been identified in mice with the mutation brachypodism (bp), a mutation which affects the length and number of bones in limbs (6). GDF-6 and GDF-7 are closely related to GDF-5 (6). GDF-8 has been shown to be a negative regulator of skeletal muscle mass (1).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11461R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11461R-CY7
Lokale Artikelnummer::
BOSSBS-11461R-CY7
Beschreibung:
Growth/differentiation factors (GDFs) are members of the TGF superfamily (1,2). Members of the TGF superfamily are involved in embryonic development and adult tissue homeostasis (1). GDF-1 expression is almost exclusively restricted to the central nervous system and mediates cell differentiation events during embryonic development (3). Neither GDF-3 (Vgr-2) nor GDF-9 contains the conserved cysteine residue which is found in most other TGF superfamily members. GDF-3 is detectable in bone marrow, spleen, thymus and adipose tissue, whereas GDF-9 has only been detected in ovary (4). GDF-5 (also designated CDMP-1) has been shown to induce activation of plasminogen activator, thereby inducing angiogenesis. It is predominantly expressed in long bones during fetal embryonic development and is involved in bone formation. (5). GDF-5 mutations have been identified in mice with the mutation brachypodism (bp), a mutation which affects the length and number of bones in limbs (6). GDF-6 and GDF-7 are closely related to GDF-5 (6). GDF-8 has been shown to be a negative regulator of skeletal muscle mass (1).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11461R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11461R-A488
Lokale Artikelnummer::
BOSSBS-11461R-A488
Beschreibung:
Growth/differentiation factors (GDFs) are members of the TGF superfamily (1,2). Members of the TGF superfamily are involved in embryonic development and adult tissue homeostasis (1). GDF-1 expression is almost exclusively restricted to the central nervous system and mediates cell differentiation events during embryonic development (3). Neither GDF-3 (Vgr-2) nor GDF-9 contains the conserved cysteine residue which is found in most other TGF superfamily members. GDF-3 is detectable in bone marrow, spleen, thymus and adipose tissue, whereas GDF-9 has only been detected in ovary (4). GDF-5 (also designated CDMP-1) has been shown to induce activation of plasminogen activator, thereby inducing angiogenesis. It is predominantly expressed in long bones during fetal embryonic development and is involved in bone formation. (5). GDF-5 mutations have been identified in mice with the mutation brachypodism (bp), a mutation which affects the length and number of bones in limbs (6). GDF-6 and GDF-7 are closely related to GDF-5 (6). GDF-8 has been shown to be a negative regulator of skeletal muscle mass (1).
VE:
1 * 100 µl
Preis auf Anfrage
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 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.
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