Votre recherche pour: Thermostats+chauffants

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.

Référence Produit: PRSI56-193

UOM: 1 * 400 µl

Fournisseur: ProSci Inc.

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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.

Référence Produit: BOSSBS-6580R

UOM: 1 * 100 µl

Fournisseur: Bioss

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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.

Référence Produit: BOSSBS-6580R-HRP

UOM: 1 * 100 µl

Fournisseur: Bioss

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Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.4 1 * 1 Pce

Référence Produit: AESCOM524R

UOM: 1 * 1 Pce

Fournisseur: Aesculap

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Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.0 1 * 1 Pce

Référence Produit: AESCOM520R

UOM: 1 * 1 Pce

Fournisseur: Aesculap

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Description: SPECULUM NASAL, ST.CLAIR THOMPSON, 64MM 1 * 1 Pce

Référence Produit: AESCOK072R

UOM: 1 * 1 Pce

Fournisseur: Aesculap

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Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.2 1 * 1 Pce

Référence Produit: AESCOM522R

UOM: 1 * 1 Pce

Fournisseur: Aesculap

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Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.1 1 * 1 Pce

Référence Produit: AESCOM521R

UOM: 1 * 1 Pce

Fournisseur: Aesculap

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Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.3 1 * 1 Pce

Référence Produit: AESCOM523R

UOM: 1 * 1 Pce

Fournisseur: Aesculap

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Description: SPECULUM NASAL, ST.CLAIR THOMPSON, 38MM 1 * 1 Pce

Référence Produit: AESCOK070R

UOM: 1 * 1 Pce

Fournisseur: Aesculap

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Description: SPECULUM NASAL, ST.CLAIR THOMPSON, 76MM 1 * 1 Pce

Référence Produit: AESCOK073R

UOM: 1 * 1 Pce

Fournisseur: Aesculap

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Description: Potassium sulfate, en comprimés

Référence Produit: THOMAB40

UOM: 1 * 1.000 Tablet

Fournisseur: THOMPSON & CAPPER

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Description: Potassium sulfate, en comprimés, PS KJELTABS catalyseur de minéralisation

Référence Produit: THOMAA23

UOM: 1 * 1.000 Tablet

Fournisseur: THOMPSON & CAPPER

Certificats. *Promo

Description: Réactifs de catalyse Kjeldahl sous la forme pratique de comprimés, avec un large éventail de comprimés pour convenir aux applications générales et spécifiques.

Référence Produit: 705-0510

UOM: 1 * 1.000 Tablet

Fournisseur: THOMPSON & CAPPER

Certificats. *Promo

Description: Sodium sulfate, en comprimés, KJELTABS NA catalyseur de minéralisation

Référence Produit: THOMAA40

UOM: 1 * 1.000 Tablet

Fournisseur: THOMPSON & CAPPER

Certificats. *Promo

Description: SPECIAL KJELTABS AB04 1 * 1.000 Tablet

Référence Produit: THOMAB04

UOM: 1 * 1.000 Tablet

Fournisseur: THOMPSON & CAPPER

Certificats. *Promo