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Catalog Number: (THOMAA23)
Supplier: THOMPSON & CAPPER
Description: Potassium sulphate, tablets, PS KJELTABS mineralisation catalyst
UOM: 1 * 1.000 Tablet

Catalog Number: (THOMAB40)
Supplier: THOMPSON & CAPPER
Description: Potassium sulphate, tablets
UOM: 1 * 1.000 Tablet


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Catalog Number: (THOMAA40)
Supplier: THOMPSON & CAPPER
Description: Sodium sulphate, tablets, KJELTABS NA mineralisation catalyst
UOM: 1 * 1.000 Tablet

Supplier: THOMPSON & CAPPER
Description: Kjeldahl catalyst reagents in a convenient tablet form with a range of tablets to suit general and specific applications.
Catalog Number: (548-1377)
Supplier: VWR Collection
Description: Made entirely of stainless steel for maximum durability during dry heat sterilisation or autoclaving.
UOM: 1 * 1 items


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

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

Catalog Number: (BOSSBS-6580R)
Supplier: 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


Catalog Number: (BOSSBS-6580R-HRP)
Supplier: 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


Supplier: SGE Analytical Science
Description: Stand for CRS electronic and hand crimpers and decappers

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

Supplier: SGE Analytical Science
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.

Catalog Number: (MATR4106)
Supplier: THERMO MATRIX TECHNOLOGIES
Description: Matrix®, 8-channel handheld screw cap capper/decapper stand
UOM: 1 * 1 items

Environmentally Preferable


Catalog Number: (PRSI56-193)
Supplier: ProSci Inc.
Description: 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


Catalog Number: (548-0304)
Supplier: LA PHA PACK
Description: Crimping and decapping tool operated by compressed air (min. 6,2 bar).
UOM: 1 * 1 items


Catalog Number: (MATR4120-FLEX)
Supplier: THERMO MATRIX TECHNOLOGIES
Description: A full-service, automated capping and decapping solution for Thermo Scientific™ Matrix™ and Nunc™ 48 and 96 tube racks.
UOM: 1 * 1 items

New Product


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on 0800 22 33 44.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on 0800 22 33 44
Additional Documentation may be needed to purchase this item. A VWR representative will contact you if needed.
Additional Documentation may be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalogue Number listed above. If you need further assistance, please call VWR Customer Service on 0800 22 33 44.
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