U heeft gezocht op: HENKE+SASS+WOLF

Catalogus nummer: (613-2793)

Leverancier: HENKE SASS WOLF

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

UOM: 1 * 100 ST

Certificaten Sale

Catalogus nummer: (HSWA8300020446)

Leverancier: HENKE SASS WOLF

Omschrijving: 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 ST

Sale

Leverancier: HENKE SASS WOLF

Omschrijving: Steriel, voor eenmalig gebruik, driedelig, PP-schacht en zuiger, polyisopreen-stop, latexvrij.

New Product

Leverancier: HENKE SASS WOLF

Omschrijving: Voor eenmalig gebruik, tweedelig, zonder naald, PP-schacht en PE-zuiger, vrij van latex en siliconenolie. De spuiten zijn ook verkrijgbaar met speciaal ontworpen oraal uiteinde, om te voorkomen dat er per ongeluk luer-naalden of hypodermische injectienaalden worden aangesloten, in volumes van 5 of 10 ml. Incompatibel met injectienaalden. Neem voor meer informatie contact met ons op.

New Product

Leverancier: HENKE SASS WOLF

Omschrijving: Steriele naaf en naaldbescherming voor eenmalig gebruik in PP, canule in roestvrij staal. Deze naalden worden regelmatig mechanisch geanalyseerd en ervaringen van klinische onderzoeken worden teruggevoerd om productkwaliteit en -veiligheid constant te verbeteren voor een beter patiëntcomfort.

Certificaten

Catalogus nummer: (USBIW0485-01)

Leverancier: US Biological

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

UOM: 1 * 1 EA

Sale

Catalogus nummer: (USBIW0484-100)

Leverancier: US Biological

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

UOM: 1 * 100 µl

Sale

Catalogus nummer: (BOSSBS-15591R-FITC)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15591R)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15591R-A750)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15591R-A647)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15591R-A350)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15591R-A488)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15591R-A555)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15591R-A680)

Leverancier: Bioss

Omschrijving: 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

Sale

Catalogus nummer: (BOSSBS-15591R-CY7)

Leverancier: Bioss

Omschrijving: 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

Sale