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Image Unavailable-THOMAA23

Potassium sulphate, tablets, PS KJELTABS mineralisation catalyst

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

Certificates


Image Unavailable-THOMAB40

Potassium sulphate, tablets

Catalog Number: (THOMAB40)
Supplier: THOMPSON & CAPPER
Description: Potassium sulphate, tablets
UOM: 1 * 1.000 Tablet
Image Unavailable-THOMAA40

Sodium sulphate, tablets, KJELTABS NA mineralisation catalyst

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

Certificates


Image Unavailable-705-0510

Kjeldahl tablets, Kjeltabs

Supplier: THOMPSON & CAPPER
Description: Kjeldahl catalyst reagents in a convenient tablet form with a range of tablets to suit general and specific applications.

Certificates

Product Image-548-0501

VWR®, Crimping Heads for Pneumatic Handheld Crimping Tools

Catalog Number: (548-0501)
Supplier: VWR Collection
Description: VWR®, Crimping head for 13 mm flip-top/flip-off seals
UOM: 1 * 1 items
Product Image-548-1377

VWR® Cleanroom Crimping Tools

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
Image Unavailable-SGEA311991

Crimpers and Decappers

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.

Image Unavailable-BOSSBS-6580R

Anti-GDF5 Rabbit Polyclonal Antibody

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
Product Image-548-0071

VWR®, Crimpers and Decappers

Supplier: VWR Collection
Description: Manual crimping tools.

Image Unavailable-BOSSBS-6580R-HRP

Anti-GDF5 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

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
Product Image-548-0070A

VWR®, Manual Crimper and Decapper

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

Image Unavailable-SGEA6A13D0

Electronic Battery Crimping Tools

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.

Image Unavailable-SGEA5ABAS0

Accessories for High-Power Electronic Crimpers and Decappers

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

Image Unavailable-SGEA313955

High-Power Electronic Crimpers and Decappers

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.

Product Image-MATR4106

Accessories for 8-channel screw cap capper/decapper

Catalog Number: (MATR4106)
Supplier: MATRIX TECHNOLOGIES CORP. LTD
Description: Matrix®, 8-channel handheld screw cap capper/decapper stand
UOM: 1 * 1 items
Product Image-BOCH12968

Decappers

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

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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 +353 1 88 22222.
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 +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
-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 Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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