Hai cercato: THOMPSON+

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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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: (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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Codice catalogo: (THOMAB40)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AB40

Codice articolo locale: THOMAB40

Descrizione: Potassio solfato, in pastiglie

UOM: 1 * 1 Cad.

Promo

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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Fornitore: THOMPSON & CAPPER

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

Certificati

Codice catalogo: (THOMAA12)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AA12

Codice articolo locale: THOMAA12

Descrizione: KJELTABS SX 1 * 1 Cad.

UOM: 1 * 1 Cad.

Promo

Codice catalogo: (THOMAA45)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AA45

Codice articolo locale: THOMAA45

Descrizione: KJELTABS KPC 1 * 1 Cad.

UOM: 1 * 1 Cad.

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Codice catalogo: (THOMAB61)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AB61

Codice articolo locale: THOMAB61

Descrizione: KJELTABS SPECIAL AB61 1 * 1 Cad.

UOM: 1 * 1 Cad.

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Codice catalogo: (THOMAB21)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AB21

Codice articolo locale: THOMAB21

Descrizione: [EN]SPECIAL KJELTAB AB21 1 * 1 Cad.

UOM: 1 * 1 Cad.

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Codice catalogo: (THOMAB90)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AB90

Codice articolo locale: THOMAB90

Descrizione: TAB SPECIAL KJELAB90 1 * 1 Cad.

UOM: 1 * 1 Cad.

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Codice catalogo: (THOMAB04)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AB04

Codice articolo locale: THOMAB04

Descrizione: SPECIAL KJELTABS AB04 1 * 1 Cad.

UOM: 1 * 1 Cad.

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Codice catalogo: (THOMAB42)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AB42

Codice articolo locale: THOMAB42

Descrizione: SPECIAL KJELTABS AB42 1 * 1 Cad.

UOM: 1 * 1 Cad.

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Codice catalogo: (THOMAB24)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AB24

Codice articolo locale: THOMAB24

Descrizione: [EN]SPECIAL KJELTAB AB24 1 * 1 Cad.

UOM: 1 * 1 Cad.

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Codice catalogo: (THOMAA42)

Fornitore: THOMPSON & CAPPER

Codice articolo fornitore: AA42

Codice articolo locale: THOMAA42

Descrizione: KJELTABS NAC 1 * 1 Cad.

UOM: 1 * 1 Cad.

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