Procurou por: Estearato+de+sódio

Código de Artigo: (613-2793)

Fornecedor: HENKE SASS WOLF

Descrição: These syringes are commonly used for embryo transfer and oocyte handling.

UOM: 1 * 100 unid.

Certificados Promoção

Fornecedor: HENKE SASS WOLF

Descrição: Descartáveis, de 3 peças, cilindro e êmbolo de PP, rolha de poliisopreno, isentas de látex.

Novo produto

Código de Artigo: (HSWA8300020446)

Fornecedor: HENKE SASS WOLF

Descrição: These safety needles are compatible with HENKE-JECT® syringes as well as all others syringes with Luer and Luer lock according to ISO 594.

UOM: 1 * 100 unid.

Promoção

Fornecedor: HENKE SASS WOLF

Descrição: Disposable, two-piece, without needle, PP barrel and PE piston, latex- and silicone oil-free. Syringes are also available with especially designed oral tip, which prevents accidental Luer or hypodermic connection, in volumes of 5 or 10 ml. Incompatible with injection needles. Please enquire for details.

Novo produto

Fornecedor: HENKE SASS WOLF

Descrição: Estéreis, descartáveis, adaptador e tampa da agulha em PP, cânula em aço inoxidável. Estas agulhas são analisadas mecanicamente com regularidade e as experiências obtidas na prática clínica são reportadas para assegurar um aperfeiçoamento contínuo da qualidade e segurança do produto para maior conforto do paciente.

Certificados

Código de Artigo: (USBIW0485-01)

Fornecedor: US Biological

Descrição: Anti-Wolf-Hirschhorn Syndrome Candidate 2 Protein Chicken Polyclonal Antibody

UOM: 1 * 50 µG

Promoção

Código de Artigo: (USBIW0484-100)

Fornecedor: US Biological

Descrição: Anti-Wolf-Hirschhorn Syndrome Candidate 1-like 1 Mouse Monoclonal Antibody [clone: 8G3]

UOM: 1 * 100 µl

Promoção

Código de Artigo: (USBIW0485-02)

Fornecedor: US Biological

Descrição: Anti-Wolf-Hirschhorn Syndrome Candidate 2 Protein Chicken Polyclonal Antibody

UOM: 1 * 50 µG

Promoção

Código de Artigo: (BOSSBS-15591R-FITC)

Fornecedor: Bioss

Descrição: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

UOM: 1 * 100 µl

Promoção

Código de Artigo: (USBI135380)

Fornecedor: US Biological

Descrição: Anti-WHSC1L1 Mouse Polyclonal Antibody

UOM: 1 * 50 µG

Promoção

Código de Artigo: (BOSSBS-15591R)

Fornecedor: Bioss

Descrição: This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq, Oct 2009].

UOM: 1 * 100 µl

Promoção

Código de Artigo: (BOSSBS-15591R-CY7)

Fornecedor: Bioss

Descrição: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

UOM: 1 * 100 µl

Promoção

Código de Artigo: (BOSSBS-15591R-CY3)

Fornecedor: Bioss

Descrição: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

UOM: 1 * 100 µl

Promoção

Código de Artigo: (BOSSBS-15591R-A647)

Fornecedor: Bioss

Descrição: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

UOM: 1 * 100 µl

Promoção

Código de Artigo: (BOSSBS-15591R-A750)

Fornecedor: Bioss

Descrição: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

UOM: 1 * 100 µl

Promoção

Código de Artigo: (BOSSBS-15591R-A350)

Fornecedor: Bioss

Descrição: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

UOM: 1 * 100 µl

Promoção