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Artikel-Nr: (BOSSBS-6580R-HRP)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-6580R-HRP

Beschreibung: 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

Sale

Artikel-Nr: (BOSSBS-6580R)

Lieferant: Bioss

Hersteller Artikel Nummer : BS-6580R

Beschreibung: 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

Sale

Lieferant: MACHEREY-NAGEL

Beschreibung: QUANTOFIX® Teststäbchen erfüllen alle Anforderungen an einen modernen Schnelltest. Je nach Konzentration des Analyten in der Probe ändert sich die Farbe des Indikatorfeldes. Die Auswertung erfolgt meist visuell durch einen Vergleich der Reaktionsfarbe mit der mehrstufigen Farbskala. Diese Teststreifen sind unmittelbar gebrauchsfertig. Sie erfordern kein weiteres Zubehör. Die Teststäbchen sind für die einmalige Verwendung vorgesehen und müssen weder gewartet noch kalibriert werden.

Sicherheitsdatenblätter

Artikel-Nr: (THOMAB40)

Lieferant: THOMPSON & CAPPER

Hersteller Artikel Nummer : AB40

Beschreibung: Kaliumsulfat, Tabletten

UOM: 1 * 1 Cad.

Sale

Lieferant: TENAK AS

Beschreibung: Colored cryoboxes possible to orient in different ways for classic colour coding, tracking work in progress, identifying the owner of the box, and monitoring sample thawing.

Artikel-Nr: (THOMAA23)

Lieferant: THOMPSON & CAPPER

Hersteller Artikel Nummer : AA23

Beschreibung: Kaliumsulfat, Tabletten, PS KJELTABS Mineralisierungskatalysator

UOM: 1 * 1 Cad.

Zertifikate Sale

Artikel-Nr: (PRSI56-193)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 56-193

Beschreibung: 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

New Product Sale

Artikel-Nr: (THOMAA40)

Lieferant: THOMPSON & CAPPER

Hersteller Artikel Nummer : AA40

Beschreibung: Natriumsulfat, Tabletten, KJELTABS NA Mineralisierungskatalysator

UOM: 1 * 1 Cad.

Zertifikate Sale

Lieferant: THOMPSON & CAPPER

Beschreibung: Kjeldahl-Katalysator-Reagenzien in einer praktischen Tablettenform mit einer Reihe von Tabletten für allgemeine und spezifische Anwendungen.

Zertifikate

Lieferant: VWR Chemicals

Beschreibung: VWR® <i>Taq</i> Plus is an optimised format of <i>Taq</i> DNA polymerase master mix and, therefore, is a good alternative to <i>Taq</i> DNA polymerase and <i>Taq</i> DNA polymerase master mix.

Lieferant: VWR Chemicals

Beschreibung: VWR® Probe qPCR Master Mix features a distinctive universal passive reference dye that is compatible with ROX-dependent and ROX-independent qPCR instruments.

Sicherheitsdatenblätter Zertifikate Sale

Lieferant: VWR Chemicals

Beschreibung: TEMPase Hot Start DNA Polymerase Master Mix and Blue TEMPase Master Mix are good alternatives to TEMPase Hot Start DNA Polymerase. These master mixes offer easy reaction assembly at room temperature, reduced set-up time and fewer handling steps, which lead to increased reproducibility. As a consequence TEMPase Hot Start DNA Polymerase Master Mix is highly suited to standard tests.

Lieferant: VWR Chemicals

Beschreibung: VWR® qPCR Master Mix features a distinctive universal passive reference dye that is compatible with ROX-dependent and ROX-independent qPCR instruments.

Sicherheitsdatenblätter Zertifikate Sale

Artikel-Nr: (1B1409-100RXN)

Lieferant: VWR Chemicals

Beschreibung: Hot Start PCR-To-Gel Taq Master Mix, 2X is a ready to use reaction cocktail that contains all required components, except primers and template DNA, for routine PCR amplification of DNA fragments up to 4 kb.

UOM: 1 * 1 KIT

Sicherheitsdatenblätter Sale

Lieferant: VWR Chemicals

Beschreibung: VWR® Probe One-Step RT-qPCR Master Mix with UDG is designed for the detection and quantitation of RNA targets and is an ideal choice for multiplex applications. It features a distinctive universal passive reference dye that is compatible with ROX-dependent and ROX-independent qPCR instruments.

Sicherheitsdatenblätter Zertifikate Sale

Lieferant: VWR Chemicals

Beschreibung: VWR® Red <i>Taq</i> DNA Polymerase Master Mix, which also contains an inert red dye, can be directly loaded onto an agarose gel without addition of electrophoresis loading buffers.