Print…

Procurou por: Expressão+de+proteínas


139 562  resultados encontrados

Filtrar resultados Ordenar por
SearchResultCount:"139562"

Sort Results

Visualização em Lista Easy View (new)

Classifique os resultados da pesquisa

Imagem do Produto-RPN810

Marcadores de Western blotting, ECL™ DualVue™ Amersham

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
Imagem do Produto-7190-05

Embalagens de preparação de poros largos, J.T. Baker® BAKERBOND®

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.

Imagem do Produto-83603.290

VWR®, Soluções de limpeza para elétrodos

Fornecedor: VWR Chemicals
Descrição: Para obter a informação completa sobre saúde e segurança, consulte.

MSDS Certificados

Image Unavailable-BOSSBS-3696R-CY3

Anti-MLLT10 Rabbit Polyclonal Antibody (Cy3®)

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
Imagem do Produto-101000011.

Kit de transfecção de ADN para produção de proteínas, sistema de expressão FectoCHO®

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®.

Image Unavailable-BOSSBS-9551R-HRP

Anti-BEND2 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

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
Image Unavailable-BOSSBS-9551R-CY7

Anti-BEND2 Rabbit Polyclonal Antibody (Cy7®)

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
Image Unavailable-BOSSBS-9551R-A350

Anti-BEND2 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

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
Image Unavailable-BOSSBS-9551R-A488

Anti-BEND2 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

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
Image Unavailable-BOSSBS-9551R-CY3

Anti-BEND2 Rabbit Polyclonal Antibody (Cy3®)

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
Image Unavailable-BOSSBS-8438R

Anti-BEND4 Rabbit Polyclonal Antibody

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
Imagem do Produto-516-9757

Membranas de transferência, FluoroTrans® PVDF

Fornecedor: Cytiva (Formerly Pall Lab)
Descrição: De PVDF naturalmente hidrófobo, ideais para uma grande variedade de aplicações de análise proteica. A família de membranas FluroTrans® é constituída por suportes de fase sólida microporosos brancos que unem as proteínas por interacções hidrofóbicas. A membrana FluoroTrans® está optimizada para a sequenciação de proteínas N-terminais. A membrana FluoroTrans® W está optimizada para aplicações de transferência Western. A membrana FluoroTrans® W permite a detecção de proteínas com baixo ruído de fundo e com baixa probabilidade de passar além da membrana. As proteínas imobilizadas podem ser detectadas visualmente com azul de Coomassie®, amido negro, Ponceau S e ouro coloidal.

Image Unavailable-BOSSBS-8438R-A555

Anti-BEND4 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Código de Artigo: (BOSSBS-8438R-A555)
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
Image Unavailable-BOSSBS-8438R-A488

Anti-BEND4 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Código de Artigo: (BOSSBS-8438R-A488)
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
Image Unavailable-BOSSBS-3696R-HRP

Anti-MLLT10 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

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
Image Unavailable-BOSSBS-3696R-A647

Anti-MLLT10 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

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
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.
353 - 368 of 139 562
no targeter for Bottom