Hai cercato: THOMPSON+&+CAPPER

Codice catalogo: (THOMAA23)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AA23

Codice articolo locale: THOMAA23

Descrizione: Potassio solfato, in pastiglie, PS KJELTABS catalizzatore di mineralizzazione

UOM: 1 * 1 Cad.

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Codice catalogo: (THOMAB40)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AB40

Codice articolo locale: THOMAB40

Descrizione: Potassio solfato, in pastiglie

UOM: 1 * 1 Cad.

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Fornitore: THOMPSON & CAPPER

Descrizione: Reagenti di catalizzazione Kjeldahl in pratiche compresse con una gamma adatta per applicazioni generiche e specifiche.

Certificati

Codice catalogo: (THOMAA40)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AA40

Codice articolo locale: THOMAA40

Descrizione: Sodio solfato, in pastiglie, KJELTABS NA catalizzatore di mineralizzazione

UOM: 1 * 1 Cad.

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Codice catalogo: (548-0501)

Fornitore: VWR Collection

Codice articolo locale: VWRI548-0501

Descrizione: VWR®, Testa di chiusura per ghiere Flip Top/Flip Off seals da 13 mm

UOM: 1 * 1 pezzi

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Codice catalogo: (548-1377)

Fornitore: VWR Collection

Codice articolo locale: VWRI548-1377

Descrizione: Realizzati interamente in acciaio inox per garantire la durata massima in operazioni di sterilizzazione a calore secco o autoclavaggio.

UOM: 1 * 1 pezzi

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Codice catalogo: (BOSSBS-6580R)

Fornitore: Bioss

Codice articolo fornitore: BS-6580R

Codice articolo locale: BOSSBS-6580R

Descrizione: 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

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Codice catalogo: (BOSSBS-6580R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-6580R-HRP

Codice articolo locale: BOSSBS-6580R-HRP

Descrizione: 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

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Fornitore: VWR Collection

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

Fornitore: VWR Collection

Descrizione: Manual crimping tools.

Fornitore: SGE Analytical Science

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

Fornitore: SGE Analytical Science

Descrizione: Stand for CRS electronic and hand crimpers and decappers

Fornitore: SGE Analytical Science

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

Fornitore: SGE Analytical Science

Descrizione: 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.

Codice catalogo: (BOCH12968)

Fornitore: BOCHEM

Codice articolo fornitore: 12968

Codice articolo locale: BOCH12968

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

UOM: 1 * 1 pezzi

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Codice catalogo: (PRSI56-193)

Fornitore: ProSci Inc.

Codice articolo fornitore: 56-193

Codice articolo locale: PRSI56-193

Descrizione: 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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