Votre recherche pour: THOMPSON+&+CAPPER

Référence Produit: (THOMAA23)

Fournisseur: THOMPSON & CAPPER

Description: Potassium sulfate, en comprimés, PS KJELTABS catalyseur de minéralisation

UOM: 1 * 1.000 Tablet

Certificats. *Promo

Référence Produit: (THOMAB40)

Fournisseur: THOMPSON & CAPPER

Description: Potassium sulfate, en comprimés

UOM: 1 * 1.000 Tablet

*Promo

Référence Produit: (THOMAA40)

Fournisseur: THOMPSON & CAPPER

Description: Sodium sulfate, en comprimés, KJELTABS NA catalyseur de minéralisation

UOM: 1 * 1.000 Tablet

Certificats. *Promo

Fournisseur: THOMPSON & CAPPER

Description: Réactifs de catalyse Kjeldahl sous la forme pratique de comprimés, avec un large éventail de comprimés pour convenir aux applications générales et spécifiques.

Certificats.

Fournisseur: VWR Collection

Description: Crimpers and decappers are an ideal supplement to the headspace and crimp neck vials.

Fournisseur: Trajan Scientific and Medical

Description: Crimping tools have advanced the standards of manual crimpers and decappers by addressing all of the deficiencies associated with traditional blocky, metal tools.

Fournisseur: Trajan Scientific and Medical

Description: Stand for CRS electronic and hand crimpers and decappers

Fournisseur: Trajan Scientific and Medical

Description: Electronic battery crimping tools effortlessly crimp/decap aluminum and 2-part aluminum/steel caps with just the push of a button.

Fournisseur: Trajan Scientific and Medical

Description: Ergonomic electronic high power crimping tools can effortlessly crimp/decap even the strongest all-steel caps with just the push of a button. The high power unit is designed as a single tool with interchangeable jawsets for the various functions and sizes needed in your laboratory.

Référence Produit: (BOSSBS-6580R)

Fournisseur: Bioss

Description: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.

UOM: 1 * 100 µl

*Promo

Référence Produit: (MATR4106)

Fournisseur: THERMO MATRIX TECHNOLOGIES

Description: Matrix®, Support pour pince manuelle à sertir/dessertir les bouchons à vis 8 canaux

UOM: 1 * 1 Pce

*Promo

Référence Produit: (BOCH12968)

Fournisseur: BOCHEM

Description: These decappers are used to remove aluminium crimp caps.

UOM: 1 * 1 Pce

*Promo

Référence Produit: (MMMPMDSCDL)

Fournisseur: 3M Food Safety

Description: Molecular detection cap/decap tool - Lysis

UOM: 1 * 1 KIT

*Promo

Référence Produit: (BOSSBS-6580R-HRP)

Fournisseur: Bioss

Description: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.

UOM: 1 * 100 µl

*Promo

Référence Produit: (732-4817)

Fournisseur: Thermo Fisher Scientific

Description: Conçu pour aider les utilisateurs à installer des bouchons bombés sur des plaques et des barrettes de tubes.

UOM: 1 * 1 Pce

*Promo

Fournisseur: Thermo Fisher Scientific

Description: Use SureSTART™ level 3 manual vial crimpers for 20 mm Crimp vials to ensure that your crimp caps are sealed reliably every time.