Print…

Procurou por: u0087


116  resultados encontrados

Sort Results

Visualização em Lista Easy View (new)
SearchResultCount:"116"
Descrição: These syringes are commonly used for embryo transfer and oocyte handling.
Código de Artigo: 613-2793
UOM: 1 * 100 unid.
Fornecedor: HENKE SASS WOLF

Certificados


Descrição: Descartáveis, de 3 peças, cilindro e êmbolo de PP, rolha de poliisopreno, isentas de látex.
Código de Artigo: HSWA8300065157
UOM: 1 * 1.700 unid.
Fornecedor: HENKE SASS WOLF

Novo produto


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.
Código de Artigo: HSWA8300020446
UOM: 1 * 100 unid.
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.
Código de Artigo: HSWA8300063458
UOM: 1 * 100 unid.
Fornecedor: HENKE SASS WOLF

Novo produto


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.
Código de Artigo: HSWA8300010721
UOM: 1 * 100 unid.
Fornecedor: HENKE SASS WOLF

Certificados


Descrição: Anti-Wolf-Hirschhorn Syndrome Candidate 2 Protein Chicken Polyclonal Antibody
Código de Artigo: USBIW0485-01
UOM: 1 * 50 µG
Fornecedor: US Biological


Descrição: Anti-Wolf-Hirschhorn Syndrome Candidate 1-like 1 Mouse Monoclonal Antibody [clone: 8G3]
Código de Artigo: USBIW0484-100
UOM: 1 * 100 µl
Fornecedor: US Biological


Descrição: Anti-Wolf-Hirschhorn Syndrome Candidate 2 Protein Chicken Polyclonal Antibody
Código de Artigo: USBIW0485-02
UOM: 1 * 50 µG
Fornecedor: US Biological


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.
Código de Artigo: BOSSBS-15591R-FITC
UOM: 1 * 100 µl
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].
Código de Artigo: BOSSBS-15591R
UOM: 1 * 100 µl
Fornecedor: Bioss


Descrição: Anti-WHSC1L1 Mouse Polyclonal Antibody
Código de Artigo: USBI135380
UOM: 1 * 50 µG
Fornecedor: US Biological


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.
Código de Artigo: BOSSBS-15591R-CY7
UOM: 1 * 100 µl
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.
Código de Artigo: BOSSBS-15591R-CY3
UOM: 1 * 100 µl
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.
Código de Artigo: BOSSBS-15591R-A647
UOM: 1 * 100 µl
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.
Código de Artigo: BOSSBS-15591R-A750
UOM: 1 * 100 µl
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.
Código de Artigo: BOSSBS-15591R-A350
UOM: 1 * 100 µl
Fornecedor: Bioss