Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localised to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localised to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: Bioss

This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

Supplier: HARVARD APPARATUS

The Gemini cautery system is the perfect tool for cauterising needs.

Supplier: HARVARD APPARATUS

Dual plate rotator with variable rotation rates, can be used with the Harvard apparatus 96-well equilibrium dialyser. The rotator speeds up the equilibrium dialysis process by keeping the sample in constant motion thereby ensuring higher reproducibility of results.

Supplier: HARVARD APPARATUS

Stainless steel.

Supplier: HARVARD APPARATUS

Activated charcoal canister that is designed to optimise halogenated gas absorption. Fluosorber is factory tested with an air flow of 60 LPM to ensure resistance is not above 2 cm H₂O.

Supplier: HARVARD APPARATUS

The single use 96-well DispoDialyzer™ is ideal for the simultaneous preparation of 96 samples.

Supplier: HARVARD APPARATUS

Two moving jaws with fixed screw action. The clamps mount either a closed connector, an open-sided connector or a tee connector.

Supplier: HARVARD APPARATUS

This Autoclip® wound closure system provides a rapid, easy to use method to securely close wounds. When the wound is healed, simply remove the clip using the handy removal forcep.

Supplier: HARVARD APPARATUS

Capillary tubes, made of high quality borosilicate glass with filaments.

Supplier: HARVARD APPARATUS

The Pump 11 Elite series sets a new standard for handling the challenges of new applications. It has served the research community as the work horse infusion pump for micro and macro fluidic applications including MS calibration, reactor dosing, animal drug/nutritional studies, cell injections, electrospinning and more.

Supplier: HARVARD APPARATUS

Micro dissecting forceps with tower tip. Made from stainless steel or Inox steel.

Supplier: HARVARD APPARATUS

This easily operated hole punching device is suitable for marking small rodents whenever a permanent identification system is required. Two types of punches are available. A forceps type which provides a longer handle for gripping, or the simple thumb type.

Supplier: HARVARD APPARATUS

These burette clamps are made from precision injection molded nylon with 30% glass fiber reinforcement which provides enormous strength at a great saving in weight.

Supplier: HARVARD APPARATUS

The PHD 22/2000 syringe pump series gives you the lowest flow rates, the highest accuracy, the smoothest flow, advanced programmability from the keypad. Ideal for applications in drug/nutritional delivery, electrospinning, microfluidics/nanofluidics and mass spec calibration.

Supplier: HARVARD APPARATUS

These clamps are mounted vertically 100 mm apart to hold firmly in two places condensers, large columns, large tubes, etc. The jaws open to 85 mm. To be used with either the EC1 53-2012 closed connector, EC1 53-2022 open-sided connector or the EC1 53-2032 tee connector.

Supplier: HARVARD APPARATUS

The small syringe multi-rack option will accommodate up to six 30 to 60 ml syringes or up to ten 0.5 µl to 20 ml syringes.

Supplier: HARVARD APPARATUS

Ultra-Micro SpinColumns are best suited for sample volumes from 10 to 25 µl. Centrifugation or filtration under vacuum or pressure can be used to run the sample through the columns.

Supplier: HARVARD APPARATUS

QuikPrep® SpinColumns™ with activated charcoal packing materials can be used for DNA, protein and peptide purification, small molecule, carbohydrate, salt and radiolabel removal, nick translation and affinity separation. Activated charcoal retains polar solutes. Salt will not be retained.