Hledali jste: THOMPSON+&+CAPPER

Katalogové číslo: (MATR4106)

Dodavatel: THERMO MATRIX TECHNOLOGIES

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

Měrná jednotka: 1 * 1 KS

Akce

Dodavatel: THERMO MATRIX TECHNOLOGIES

Popis: <p>Tento uzávěr/odvíčkovač umožňuje ergonomické ruční zpracování plného stojanu zkumavek Matrix® nebo Nunc™ Cryobank nebo Bank-It™ za méně než jednu minutu. Navrženo pro uzavírání zkumavek optimálním točivým momentem pro zachování integrity vzorku a zabránění ztrátě vzorku během skladování.</p>

Akce

Katalogové číslo: (MATR4111MAT-IS)

Dodavatel: THERMO MATRIX TECHNOLOGIES

Popis: The Capit-All and Capit-All IS instruments remove and replace screw caps on 96 and 24 format storage tubes with precision and ease. The instruments' robust design ensures reliable, high throughput access and storage of samples in screw cap storage tubes, while reducing risk of repetitive strain injury.

Měrná jednotka: 1 * 1 KS

Akce

Katalogové číslo: (KACC032TWE)

Dodavatel: KEYSTONE CLEANROOM PRODUCTS

Popis: [EN]COVER 32 WHITE FOR CAPPER BOWL 1 * 50 KS

Měrná jednotka: 1 * 50 KS

New Product Akce

Katalogové číslo: (KACC3034TWELTT)

Dodavatel: KEYSTONE CLEANROOM PRODUCTS

Popis: [EN]FLAT SHEET CAPPER HOPPER ALEXION 1 * 50 KS

Měrná jednotka: 1 * 50 KS

New Product Akce

Katalogové číslo: (PRSI56-193)

Dodavatel: ProSci Inc.

Popis: 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.

Měrná jednotka: 1 * 400 µl

Akce

Katalogové číslo: (BOSSBS-6580R)

Dodavatel: Bioss

Popis: 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.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-6580R-HRP)

Dodavatel: Bioss

Popis: 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.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (THOMAA23)

Dodavatel: THOMPSON & CAPPER

Popis: Síran draselný, tablets, PS KJELTABS mineralisation catalyst

Měrná jednotka: 1 * 1.000 Tablet

Certifikáty Akce

Katalogové číslo: (THOMAB40)

Dodavatel: THOMPSON & CAPPER

Popis: Síran draselný, tablets

Měrná jednotka: 1 * 1.000 Tablet

Akce

Dodavatel: THOMPSON & CAPPER

Popis: Kjeldahl catalyst reagents in a convenient tablet form with a range of tablets to suit general and specific applications.

Certifikáty

Katalogové číslo: (THOMAA40)

Dodavatel: THOMPSON & CAPPER

Popis: Síran sodný, tablets, KJELTABS NA mineralisation catalyst

Měrná jednotka: 1 * 1.000 Tablet

Certifikáty Akce

Dodavatel: VWR Collection

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

Dodavatel: Trajan Scientific and Medical

Popis: Stand for CRS electronic and hand crimpers and decappers

Dodavatel: Trajan Scientific and Medical

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

Katalogové číslo: (MATR4109)

Dodavatel: THERMO MATRIX TECHNOLOGIES

Popis: [EN]CAPPER/DECAPPER SPARE POWER SUPPLY 1 * 1 KS

Měrná jednotka: 1 * 1 KS

Akce