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Procurou por: Expressão+de+proteínas


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Fornecedor: Merck Millipore (Novagen)
Descrição: O reagente para extracção de proteínas BugBuster® Protein foi formulado de modo a fraccionar suavemente a parede das células de <i>E. coli</i>, libertando proteína solúvel. Constitui uma alternativa simples, rápida e económica a métodos mecânicos como, p. ex., French Press ou sonicação, para libertar proteína alvo expressa, na preparação para a purificação ou outras aplicações. A formulação utiliza uma mistura de detergentes capaz de perfurar a parede das células sem desnaturar a proteína solúvel.

Código de Artigo: (RPN810)
Fornecedor: Cytiva
Descrição: Os marcadores de Western blotting ECL™ DualVue™ Amersham desempenham duas funções essenciais. Em primeiro lugar, as proteínas do marcador pré-corado confirmam a transferência de proteínas para além de definir claramente a orientação do blot. Em segundo lugar, as proteínas recombinantes marcadas são detetadas na película através de imagem CCD em conjunto com a(s) proteína(s) alvo de interesse, permitindo a determinação extremamente precisa da massa molecular da(s) proteína(s) alvo. Os marcadores marcados são detetados facilmente e especificamente por meio de um conjugado específico que elimina qualquer contaminação cruzada entre a(s) proteína(s) alvo e os marcadores.
UOM: 1 * 1 KIT


Fornecedor: Avantor
Descrição: Embalagens de coluna à base de sílica com purificação de alto desempenho de peptídeos e proteínas fortemente hidrófilos, com base em características hidrófobas e formas moleculares.

Código de Artigo: (BOSSBS-3696R-CY3)
Fornecedor: Bioss
Descrição: A chromosomal aberration involving MLLT10 is associated with acute leukemias. Translocation t(10;11)(p12;q23) with MLL/HRX. The result is a rogue activator protein.A chromosomal aberration involving MLLT10 is associated with diffuse histiocytic lymphomas. Translocation t(10;11)(p13;q14) with PICALM.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-9551R-A350)
Fornecedor: Bioss
Descrição: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. 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


Fornecedor: VWR Chemicals
Descrição: Para obter a informação completa sobre saúde e segurança, consulte.
Código de Artigo: (BOSSBS-9551R-HRP)
Fornecedor: Bioss
Descrição: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. 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


Código de Artigo: (BOSSBS-9551R-CY7)
Fornecedor: Bioss
Descrição: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. 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


Código de Artigo: (BOSSBS-9551R-A488)
Fornecedor: Bioss
Descrição: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. 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


Código de Artigo: (BOSSBS-9551R-CY3)
Fornecedor: Bioss
Descrição: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. 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


Código de Artigo: (BOSSBS-8438R)
Fornecedor: Bioss
Descrição: BEND4 is a 530 amino acid protein that contains a BEN domain. BEND4 exists as five alternatively spiced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND4 gene maps to human chromosome 4p13. Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-8438R-A647)
Fornecedor: Bioss
Descrição: BEND4 is a 530 amino acid protein that contains a BEN domain. BEND4 exists as five alternatively spiced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND4 gene maps to human chromosome 4p13. Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-3696R-HRP)
Fornecedor: Bioss
Descrição: A chromosomal aberration involving MLLT10 is associated with acute leukemias. Translocation t(10;11)(p12;q23) with MLL/HRX. The result is a rogue activator protein.A chromosomal aberration involving MLLT10 is associated with diffuse histiocytic lymphomas. Translocation t(10;11)(p13;q14) with PICALM.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-3696R-A647)
Fornecedor: Bioss
Descrição: A chromosomal aberration involving MLLT10 is associated with acute leukemias. Translocation t(10;11)(p12;q23) with MLL/HRX. The result is a rogue activator protein.A chromosomal aberration involving MLLT10 is associated with diffuse histiocytic lymphomas. Translocation t(10;11)(p13;q14) with PICALM.
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-3696R-CY7)
Fornecedor: Bioss
Descrição: A chromosomal aberration involving MLLT10 is associated with acute leukemias. Translocation t(10;11)(p12;q23) with MLL/HRX. The result is a rogue activator protein.A chromosomal aberration involving MLLT10 is associated with diffuse histiocytic lymphomas. Translocation t(10;11)(p13;q14) with PICALM.
UOM: 1 * 100 µl


Fornecedor: Polyplus-transfection
Descrição: FectoCHO® expression system consists in the synergistic association of a novel CHO chemically defined medium, FectoCHO® CD expression medium and a powerful transfection reagent, FectoPRO®.

Preço sob consulta
O stock para este item é limitado. Por favor, certifique-se de que efetuou o seu login para visualizar o stock disponível. Se a call ainda é exibida e precisar de ajuda, por favor, ligue para 213 600 770
O stock para este item é limitado. Por favor, certifique-se de que efetuou o seu login para visualizar o stock disponível. Se a call está visível e precisar de ajuda, por favor, ligue para 213 600 770
Este produto é sujeito a regulamentação especifica.
Em caso de encomenda, será contactado a solicitar documentação complementar necessária e/ou obrigatória (licença, autorização ou declaração de uso final) para a continuidade do pedido. Agradecemos a vossa compreensão
Este produto é sujeito a regulamentação especifica.
Em caso de encomenda, será contactado a solicitar documentação complementar necessária e/ou obrigatória (licença, autorização ou declaração de uso final) para a continuidade do pedido. Agradecemos a vossa compreensão.
Este produto está bloqueado. Para obter mais informações, contacte a VWR através do número 213 600 770.
O produto pretendido já não se encontra disponível. O produto indicado é um substituto.
Este produto encontra-se em rutura de stock. Poderá encontrar alternativas pesquisando pelo código de artigo indicado acima. Se precisar de ajuda, por favor contacte a VWR através do 213 600 770.
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