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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-548-1377

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
Product Image-548-0069A

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-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
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
Image Unavailable-SGEA313990

Crimpers and Decappers

Supplier: SGE a Trajan company
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-SGEA5ABAS0

Accessories for High-Power Electronic Crimpers and Decappers

Supplier: SGE a Trajan company
Description: Stand for CRS electronic and hand crimpers and decappers

Image Unavailable-SGEA6A11D0

Electronic Battery Crimping Tools

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

Image Unavailable-SGEA320955

High-Power Electronic Crimpers and Decappers

Supplier: SGE a Trajan company
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-BOCH12968

Decappers

Catalog Number: (BOCH12968)
Supplier: BOCHEM
Description: These decappers are used to remove aluminium crimp caps.
UOM: 1 * 1 items
Product Image-MMMPMDSCDL

Molecular detection cap/decap tool - lysis

Catalog Number: (MMMPMDSCDL)
Supplier: 3M Food Safety
Description: Molecular detection cap/decap tool - Lysis
UOM: 1 * 1 KIT
Product Image-732-4817

Capping tool, Cap-It

Catalog Number: (732-4817)
Supplier: Thermo Fisher Scientific
Description: Designed to assist users in applying domed caps to tube strips and plates.
UOM: 1 * 1 items
Product Image-PRSI56-193

Anti-GDF5 Rabbit Polyclonal Antibody

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

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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 at +43 1 97002 - 0.
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 at +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at +43 1 97002 - 0.
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