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Image Unavailable-BOSSBS-8309R-CY3

Anti-ANKRD54 Rabbit Polyclonal Antibody (Cy3®)

Descripción: ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. 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-8309R-CY3
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-9987R-A750

Anti-C22orf9 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Descripción: C22orf9 is a 404 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chromosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukaemia.
Numero del catalogo: BOSSBS-9987R-A750
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-9073R-A647

Anti-C22ORF31 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descripción: C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia.
Numero del catalogo: BOSSBS-9073R-A647
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-9073R-CY5

Anti-C22ORF31 Rabbit Polyclonal Antibody (Cy5®)

Descripción: C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia.
Numero del catalogo: BOSSBS-9073R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-9073R-A680

Anti-C22orf31 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Descripción: C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia.
Numero del catalogo: BOSSBS-9073R-A680
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-9986R-A680

Anti-C22orf36 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Descripción: C22orf36 is a 315 amino acid protein that contains two LRR (leucine-rich) repeats and exists as two alternatively spliced isoforms. C22orf36 is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chromosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukaemia.
Numero del catalogo: BOSSBS-9986R-A680
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-TCIAC1546-25G

Ethyl-2-cyano-2-methylpropionate ≥98.0% (por GC)

Descripción: Ethyl-2-cyano-2-methylpropionate ≥98.0% (por GC)
Numero del catalogo: TCIAC1546-25G
UOM: 1 * 25 g
Proveedor: TCI
Image Unavailable-BOSSBS-8079R-A680

Anti-CCDC134 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Descripción: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.
Numero del catalogo: BOSSBS-8079R-A680
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-8079R-A555

Anti-CCDC134 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Descripción: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.
Numero del catalogo: BOSSBS-8079R-A555
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-15140R-CY5

Anti-C22orf43 Rabbit Polyclonal Antibody (Cy5®)

Descripción: C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia.
Numero del catalogo: BOSSBS-15140R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-8309R-A750

Anti-ANKRD54 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Descripción: ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. 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-8309R-A750
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-TCIAT2563-200MG

Tetraethyl-4-tert-butylcalix[4]arene-O,O',O'',O'''-tetraacetate ≥96.0% (by HPLC)

Descripción: Tetraethyl-4-tert-butylcalix[4]arene-O,O',O'',O'''-tetraacetate ≥96.0% (by HPLC)
Numero del catalogo: TCIAT2563-200MG
UOM: 1 * 200 mg
Proveedor: TCI
Image Unavailable-BOSSBS-15140R-FITC

Anti-C22orf43 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Descripción: C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. 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 leukemia.
Numero del catalogo: BOSSBS-15140R-FITC
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-TCIAA3227-1G

Alizarina complexona ≥70% (by HPLC)

Descripción: Alizarina complexona ≥70% (by HPLC)
Numero del catalogo: TCIAA3227-1G
UOM: 1 * 1 g
Proveedor: TCI
Image Unavailable-BOSSBS-8309R-A488

Anti-ANKRD54 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Descripción: ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. 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-8309R-A488
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-TCIAP2165-25G

Phenethyl salicylate ≥98.0% (por GC)

Descripción: Phenethyl salicylate ≥98.0% (por GC)
Numero del catalogo: TCIAP2165-25G
UOM: 1 * 25 g
Proveedor: TCI
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