You Searched For: 7-Methoxy-2-methylquinoline-3-carboxylic acid

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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

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Anti-GDF5 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-6580R-HRP)

Supplier: Bioss

UOM: 1 * 100 µl

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Potassium sulphate, tablets

Catalog Number: (THOMAB40)

Supplier: THOMPSON & CAPPER

Description: Potassium sulphate, tablets

UOM: 1 * 1.000 Tablet

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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

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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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