Sie suchten nach: THOMPSON+&+CAPPER

Artikel-Nr: (THOMAA23)

Lieferant: THOMPSON & CAPPER

Hersteller Artikel Nummer : AA23

Beschreibung: Kaliumsulfat, Tabletten, PS KJELTABS Mineralisierungskatalysator

UOM: 1 * 1 Cad.

Zertifikate Sale

Artikel-Nr: (THOMAB40)

Lieferant: THOMPSON & CAPPER

Hersteller Artikel Nummer : AB40

Beschreibung: Kaliumsulfat, Tabletten

UOM: 1 * 1 Cad.

Sale

Artikel-Nr: (THOMAA40)

Lieferant: THOMPSON & CAPPER

Hersteller Artikel Nummer : AA40

Beschreibung: Natriumsulfat, Tabletten, KJELTABS NA Mineralisierungskatalysator

UOM: 1 * 1 Cad.

Zertifikate Sale

Lieferant: THOMPSON & CAPPER

Beschreibung: Kjeldahl-Katalysator-Reagenzien in einer praktischen Tablettenform mit einer Reihe von Tabletten für allgemeine und spezifische Anwendungen.

Zertifikate

Artikel-Nr: (548-1377)

Lieferant: VWR Collection

Beschreibung: Komplett aus Edelstahl gefertigt, für maximale Haltbarkeit während der Heißluftsterilisation oder Autoklavierung.

UOM: 1 * 1 ST

Sale

Lieferant: SGE Analytical Science

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

Lieferant: VWR Collection

Beschreibung: Bördel- und Öffnungszangen sind eine ideale Ergänzung zu den Headspace- und Rollrandflaschen.

Artikel-Nr: (BOSSBS-6580R-HRP)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-6580R-HRP

Beschreibung: 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

Sale

Artikel-Nr: (BOSSBS-6580R)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-6580R

Beschreibung: 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

Sale

Lieferant: SGE Analytical Science

Beschreibung: Stand for CRS electronic and hand crimpers and decappers

Lieferant: SGE Analytical Science

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

Lieferant: SGE Analytical Science

Beschreibung: 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.

Artikel-Nr: (MATR4106)

Lieferant: THERMO MATRIX TECHNOLOGIES

Hersteller Artikel Nummer : 4106

Beschreibung: Matrix®, Rack für manuellen 8-Kanal-Capper/Decapper für Schraubverschlüsse

UOM: 1 * 1 ST

Sale

Artikel-Nr: (PRSI56-193)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 56-193

Beschreibung: The protein encoded by this gene is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. This group of proteins is characterized by a polybasic proteolytic processing site which is cleaved to produce a mature protein containing seven conserved cysteine residues. The members of this family are regulators of cell growth and differentiation in both embryonic and adult tissues. Mutations in this gene are associated with acromesomelic dysplasia, Hunter-Thompson type; brachydactyly, type C; and chondrodysplasia, Grebe type. These associations confirm that the gene product plays a role in skeletal development.

UOM: 1 * 400 µl

New Product Sale

Artikel-Nr: (548-0304)

Lieferant: LA PHA PACK

Hersteller Artikel Nummer : 00000089

Beschreibung: Werkzeug zum Verschließen und Öffnen von Bördelkappen mittels Druckluft (min. 6,2 bar).

UOM: 1 * 1 ST

Sale

Lieferant: Thermo Fisher Scientific

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