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Image Unavailable-6540-100

L(-)-Triptófano, Millipore®

Descripción: L(-)-Triptófano, Millipore®
Numero del catalogo: 6540-100
UOM: 1 * 100 g
Proveedor: Merck Millipore (Calbiochem‎)
Image Unavailable-TCIAL0038-100MG

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

Descripción: DL-Leucyl-DL-phenylalanine ≥98.0% (by titrimetric analysis)
Numero del catalogo: TCIAL0038-100MG
UOM: 1 * 100 mg
Proveedor: TCI
Image Unavailable-H56126.14

DL-Cisteína 96%

Descripción: DL-Cisteína 96%
Numero del catalogo: H56126.14
UOM: 1 * 25 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Product Image-ACRO159095000

DL-Alanina 99%

Descripción: DL-Alanina 99%
Numero del catalogo: ACRO159095000
UOM: 1 * 500 g
Proveedor: Thermo Fisher Scientific

FDS


Image Unavailable-APOSOR912027-25G

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

Descripción: DL-tert-Leucine (H-DL-Tle-OH) 97%
Numero del catalogo: APOSOR912027-25G
UOM: 1 * 25 g
Proveedor: Apollo Scientific
Image Unavailable-L09895.09

DL-Arabinosa ≥98%

Descripción: DL-Arabinosa ≥98%
Numero del catalogo: L09895.09
UOM: 1 * 10 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Image Unavailable-A10606.22

DL-Treonina ≥99%

Descripción: DL-Treonina ≥99%
Numero del catalogo: A10606.22
UOM: 1 * 100 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Image Unavailable-TCIAA0187-100MG

DL-Alanyl-DL-methionine ≥98.0% (by HPLC, titration analysis)

Descripción: DL-Alanyl-DL-methionine ≥98.0% (by HPLC, titration analysis)
Numero del catalogo: TCIAA0187-100MG
UOM: 1 * 100 mg
Proveedor: TCI
Image Unavailable-A13740.18

DL-Tirosina ≥98%

Descripción: DL-Tirosina ≥98%
Numero del catalogo: A13740.18
UOM: 1 * 50 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Image Unavailable-PRSI92-161

Human recombinant Tryptophan 5-hydroxylase 2 (from E. coli)

Descripción: Tryptophan 5-hydroxylase 2 (TPH2) is an isozyme member of the biopterin-dependent aromatic amino acid hydroxylase family. TPH2 is primarily expressed in the serotonergic neurons of the brain, with the highest expression found in the raphe nucleus of the midbrain. TPH2 catalyses the first and rate limiting step in the biosynthesis of serotonin, an important hormone and neurotransmitter. Genetic variation in TPH2 may influence susceptibility to major depressive disorder (MDD). Defects in TPH2 are the cause of psychiatric diseases such as bipolar affective disorder and major depression.
Numero del catalogo: PRSI92-161
UOM: 1 * 50 µG
Proveedor: ProSci Inc.
Image Unavailable-A16756.36

DL-Valina ≥99%

Descripción: DL-Valina ≥99%
Numero del catalogo: A16756.36
UOM: 1 * 500 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Image Unavailable-BOSSBS-0121R-A350

Anti-SYAP1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

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.
Numero del catalogo: BOSSBS-0121R-A350
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-0121R-A555

Anti-SYAP1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

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.
Numero del catalogo: BOSSBS-0121R-A555
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11489R-FITC

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

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.
Numero del catalogo: BOSSBS-11489R-FITC
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11489R-CY3

Anti-TNRC6B Rabbit Polyclonal Antibody (Cy3®)

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.
Numero del catalogo: BOSSBS-11489R-CY3
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-0121R-HRP

Anti-SYAP1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

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.
Numero del catalogo: BOSSBS-0121R-HRP
UOM: 1 * 100 µl
Proveedor: Bioss
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