Esta buscando: THOMPSON+&+CAPPER

Numero del catalogo: (THOMAA23)

Proveedor: THOMPSON & CAPPER

Descripción: Potasio sulfato, tabletas, PS KJELTABS catalizador de mineralización

UOM: 1 * 1 C/U

Certificados Promoción

Numero del catalogo: (THOMAB40)

Proveedor: THOMPSON & CAPPER

Descripción: Potasio sulfato, tabletas

UOM: 1 * 1 C/U

Promoción

Numero del catalogo: (THOMAA40)

Proveedor: THOMPSON & CAPPER

Descripción: Sodio sulfato, tabletas, KJELTABS NA catalizador de mineralización

UOM: 1 * 1 C/U

Certificados Promoción

Proveedor: THOMPSON & CAPPER

Descripción: Reactivos catalizadores Kjeldahl en forma de tableta conveniente con una gama de tabletas para adaptarse a aplicaciones generales y específicas.

Certificados

Numero del catalogo: (548-1377)

Proveedor: VWR Collection

Descripción: Fabricados totalmente de acero inoxidable para lograr la máxima duración durante la esterilización por calor seco o autoclave.

UOM: 1 * 1 UN

Promoción

Numero del catalogo: (BOSSBS-6580R-HRP)

Proveedor: Bioss

Descripción: 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

Promoción

Numero del catalogo: (BOSSBS-6580R)

Proveedor: Bioss

Descripción: 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

Promoción

Proveedor: (SGE a Trajan company)

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

Proveedor: VWR Collection

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

Proveedor: (SGE a Trajan company)

Descripción: Stand for CRS electronic and hand crimpers and decappers

Proveedor: (SGE a Trajan company)

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

Proveedor: (SGE a Trajan company)

Descripción: 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.

Numero del catalogo: (PRSI56-193)

Proveedor: ProSci Inc.

Descripción: 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 Promoción

Numero del catalogo: (MATR4106)

Proveedor: THERMO MATRIX TECHNOLOGIES

Descripción: Matrix®, 8-channel handheld screw cap capper/decapper stand

UOM: 1 * 1 UN

Promoción

Numero del catalogo: (548-0304)

Proveedor: LA PHA PACK

Descripción: Crimping and decapping tool operated by compressed air (min. 6,2 bar).

UOM: 1 * 1 UN

Promoción

Numero del catalogo: (BOCH12968)

Proveedor: BOCHEM

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

UOM: 1 * 1 UN

Promoción