Votre recherche pour: HENKE+SASS+WOLF

Référence Produit: (613-2793)

Fournisseur: HENKE SASS WOLF

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

UOM: 1 * 100 Pce

Certificats. *Promo

Référence Produit: (HSWA8300020446)

Fournisseur: HENKE SASS WOLF

Description: Ces aiguilles de sécurité sont compatibles avec les seringues HENKE-JECT®, ainsi que toutes les autres seringues avec embouts Luer et Luer Lock conformément à la norme ISO 594.

UOM: 1 * 100 Pce

*Promo

Fournisseur: HENKE SASS WOLF

Description: Seringues jetables, trois pièces, cylindre et piston en PP, bouchon en polyisoprène, sans latex.

New Product

Fournisseur: HENKE SASS WOLF

Description: À usage unique, 2 pièces, sans aiguille, cylindre en PP et piston en PE, sans latex ni huile de silicone. Les seringues sont disponibles avec un embout buccal conçu pour éviter une connexion Luer ou hypodermique accidentelle, dans des volumes de 5 ou 10 ml. Incompatibles avec les aiguilles d'injection. Pour tout complément d'information, veuillez nous contacter.

New Product

Fournisseur: HENKE SASS WOLF

Description: Embout et protection d'aiguille stérile et jetable en PP, canule en acier inoxydable. Ces aiguilles sont analysées mécaniquement de façon régulière et des expériences de pratique clinique sont réalisées afin d'améliorer en permanence la qualité et la sécurité des produits pour un meilleur confort du patient.

Référence Produit: (USBIW0485-01)

Fournisseur: US Biological

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

UOM: 1 * 50 µG

*Promo

Référence Produit: (USBIW0484-100)

Fournisseur: US Biological

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

UOM: 1 * 100 µl

*Promo

Référence Produit: (BOSSBS-15591R-FITC)

Fournisseur: Bioss

Description: 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

*Promo

Référence Produit: (USBIW0485-02)

Fournisseur: US Biological

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

UOM: 1 * 50 µG

*Promo

Référence Produit: (BOSSBS-15591R)

Fournisseur: Bioss

Description: 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

*Promo

Référence Produit: (BOSSBS-15591R-A750)

Fournisseur: Bioss

Description: 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

*Promo

Référence Produit: (BOSSBS-15591R-A647)

Fournisseur: Bioss

Description: 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

*Promo

Référence Produit: (BOSSBS-15591R-CY7)

Fournisseur: Bioss

Description: 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

*Promo

Référence Produit: (BOSSBS-15591R-CY3)

Fournisseur: Bioss

Description: 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

*Promo

Référence Produit: (BOSSBS-15591R-A350)

Fournisseur: Bioss

Description: 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

*Promo

Référence Produit: (BOSSBS-15591R-A488)

Fournisseur: Bioss

Description: 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

*Promo