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Esta buscando: 4-Bromo-DL-tryptophan


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Image Unavailable-A13740.18

DL-Tirosina ≥98%

Proveedor: Thermo Fisher Scientific
Descripción: DL-Tirosina ≥98%

FDS Certificados

Image Unavailable-BOSSBS-0121R-FITC

Anti-SYAP1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numero del catalogo: (BOSSBS-0121R-FITC)
Proveedor: Bioss
Descripción: SYAP1 (synapse-associated protein 1) is a 352 amino acid protein that is ubiquitously expressed in adult tissues. SYAP1 contains one BSD domain which is a novel domain that is present in basal transcription factors, synapse-associated proteins and several hypothetical proteins. The BSD domain is characterized by three predicted alpha helices and by conserved tryptophan and phenylalanine residues, located at the C-terminus of the domain. The gene that encodes SYAP1 in humans is located on chromosome X. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0121R-A680

Anti-SYAP1 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numero del catalogo: (BOSSBS-0121R-A680)
Proveedor: Bioss
Descripción: SYAP1 (synapse-associated protein 1) is a 352 amino acid protein that is ubiquitously expressed in adult tissues. SYAP1 contains one BSD domain which is a novel domain that is present in basal transcription factors, synapse-associated proteins and several hypothetical proteins. The BSD domain is characterised by three predicted alpha helices and by conserved tryptophan and phenylalanine residues, located at the C-terminus of the domain. The gene that encodes SYAP1 in humans is located on chromosome X. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-0121R-A750

Anti-SYAP1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Numero del catalogo: (BOSSBS-0121R-A750)
Proveedor: Bioss
Descripción: SYAP1 (synapse-associated protein 1) is a 352 amino acid protein that is ubiquitously expressed in adult tissues. SYAP1 contains one BSD domain which is a novel domain that is present in basal transcription factors, synapse-associated proteins and several hypothetical proteins. The BSD domain is characterised by three predicted alpha helices and by conserved tryptophan and phenylalanine residues, located at the C-terminus of the domain. The gene that encodes SYAP1 in humans is located on chromosome X. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
UOM: 1 * 100 µl
Product Image-PRSI26-070

Anti-TDO2 Rabbit Polyclonal Antibody

Numero del catalogo: (PRSI26-070)
Proveedor: ProSci Inc.
Descripción: Tryptophan 2,3-dioxygenase (EC 1.13.11.11) plays a role in catalyzing the first and rat-limiting step in the kynurenine pathway, the major pathway of tryptophan metabolism.
UOM: 1 * 50 µG
Image Unavailable-ICNA0210315191

L(-)-Triptófano ≥99%, en polvo

Proveedor: MP Biomedicals
Descripción: L-Tryptophan is an amino acid precursor of serotonin and melatonin.

Product Image-27925.292

DL-Lactato de sodio 60% en solución acuosa, purificado

Numero del catalogo: (27925.292)
Proveedor: VWR Chemicals
Descripción: DL-Lactato de sodio 60% en solución acuosa, purificado
UOM: 1 * 1 L

FDS Certificados


Product Image-ACRO159095000

DL-Alanina 99%

Proveedor: Thermo Fisher Scientific
Descripción: DL-Alanina 99%

FDS

Image Unavailable-APOSOR912027-25G

DL-tert-Leucine (H-DL-Tle-OH) 97%

Proveedor: Apollo Scientific
Descripción: DL-tert-Leucine (H-DL-Tle-OH) 97%

Image Unavailable-A17521.14

DL-Isoleucina ≥99%

Proveedor: Thermo Fisher Scientific
Descripción: DL-Isoleucina ≥99%

FDS Certificados

Image Unavailable-A16756.22

DL-Valina ≥99%

Proveedor: Thermo Fisher Scientific
Descripción: DL-Valina ≥99%

FDS Certificados

Product Image-ACRO164571000

DL-α-Fenilalanina 99%

Proveedor: Thermo Fisher Scientific
Descripción: DL-α-Fenilalanina 99%

FDS

Image Unavailable-TCIAA0172-25G

DL-Adrenaline ≥98.0% (by titrimetric analysis)

Proveedor: TCI
Descripción: DL-Adrenaline ≥98.0% (by titrimetric analysis)

Image Unavailable-TCIAA0223-1G

DL-Alanyl-DL-phenylalanine ≥98.0% (by titrimetric analysis)

Numero del catalogo: (TCIAA0223-1G)
Proveedor: TCI
Descripción: DL-Alanyl-DL-phenylalanine ≥98.0% (by titrimetric analysis)
UOM: 1 * 1 g
Image Unavailable-BOSSBS-11489R-FITC

Anti-TNRC6B Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numero del catalogo: (BOSSBS-11489R-FITC)
Proveedor: Bioss
Descripción: TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11489R-CY3

Anti-TNRC6B Rabbit Polyclonal Antibody (Cy3®)

Numero del catalogo: (BOSSBS-11489R-CY3)
Proveedor: Bioss
Descripción: TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
UOM: 1 * 100 µl
Consulta de precio
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta. Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta.
Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto ha sido bloqueado por su organización. Por favor, pónganse en contacto con su departamento de compras para obtener más información.
El producto original ya no está disponible. Su sustituto se muestra a continuación.
El producto(s) marcados con este símbolo están descatalogados - se venden hasta acabar stock. Pueden encontrar alternativas buscando con el número de catálogo VWR listado arriba. Si necesita más ayuda, por favor llame al Servicio de atención al cliente de VWR al 902.222.897.
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