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Crufts 2022 |
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Dear Breeder
We are pleased to announce that LABOKLIN will be at Crufts from 10th to 13th March 2022 and we look forward to seeing you there.
Our stand is located in Hall 3 opposite the restaurant, it is stand number 3-7a as shown in the diagram.
Meet the Laboklin UK team in
person
We are always talk to you on the phone, by email or even via facebook, however, at Crufts we are very excited to meet you in person and to answer any questions you have, please stop by and say hi.
10% discount on all DNA tests submitted at Crufts!
and this offer includes our Breed Specific DNA Bundles
and the brand new KC breed bundles
How to submit a sample at Crufts:
How to submit a sample at Crufts :
- Bring your dog to our stand 3-7a: we will take a DNA sample for your genetic test, all you need to do is complete the order form and pay the fees. Or,
- If you don't want to wait in the queue, you can prepare your sample in advance and bring it together with the attached order form with you to our stand. You can order a free DNA testing kit on our website, click on the following link to order:
Request sample materials
We will send you a testing kit which also contains order form and instructions on how to take DNA sample from the mouth. Prepare your sample up to a week before your planned visit, just hand the sample to us at the show.
- If you prefer to use blood for your test, ask your vet to collect 0.5-1 ml of whole blood in EDTA blood tube, bring it together with the completed order form to the show, just hand it to us. (you can order free EDTA blood tube from our website http://www.laboklin.co.uk )
Please note we will only accept Cash, Cheques or Postal Orders at the show. If you wish to pay by card, you can complete the card payment section on the order form. Paypal payments must be made in advance. Turnaround: 1-3 weeks for the majority of tests from Monday 14th March. The attached order form will only be accepted at Crufts 2022. If you have any questions, please email info@laboklin.co.uk or ring 0161 2823066. We look forward to seeing you at Crufts.
Kind regards
The Laboklin Team LABOKLIN (UK)
Laboratory For Veterinary
Diagnostics
125 Northenden Road
Manchester
M33 3HF
Tel: 0161 282 3066
Fax: 0161 973 3434
www.laboklin.co.uk
www.facebook.com/Laboklin
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new
Progressive Retinal Atrophy (JPH2 - PRA )
Progressive retinal atrophy (PRA), common autosomal recessive disorder affecting several dog breeds including Shih Tzu, is characterized by degeneration of photoreceptors leading to blindness. A mutation in the JPH2 gene has been identified to be responsible for PRA in the Shih Tzu breed and the test is now available at Laboklin.
cost £48.00
more informatrion is
available on the following link:
JPH2 - PRA in Shih Tzu
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new
Exfoliative Cutaneous Lupus Rrythematosus
( ECLE ) / Lupoid Dermatosis
Exfoliative Cutaneous Lupus Erythematosus (ECLE), which is also known as Lupoid Dermatosis is an inherited monogenic (controlled by one gene) disease that has been observed in the German Shorthaired Pointer and Hungarian Vizsla breeds. Symptoms start in the first year of age and include skin lesions, lameness, scaling, erythema (reddening of the skin), erosions/ulcers, scarring, disfiguration, decreased quality of life, progresses to joint pain, oligospermia (low sperm count) in males which progressed to azoospermia (absence of sperm), irregular heat cycles in females. Dogs with this disease have dramatically shortened life expectancies and are generally humanely euthanized upon diagnosis.
The mode of inheritance is autosomal recessive, which means that the disease occur when the puppy inherits two copies of the mutation, one from each parent.
cost £48.00
more informatrion is
available on the following link:
Exfoliative Cutaneous Lupus Rrythematosus ( ECLE )
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new
Dilated Cardiac Myopathy (DCM)
The disease is characterized by
a swelling of one or both of the
hearts ventricles (lower
chambers) which weakens the
ability of the heart to pump
blood and consequently the heart
becomes larger and the beats
become weaker. Symptoms can vary
in the different breeds. Some
affected dogs may not exhibit
any visible signs and yet die
suddenly without warning, or may
not show any symptoms for years,
however, eventually, start
exhibiting symptoms of ill
health including: lethargy, loss
of appetite, coughing especially
during exercise, gasping for
breath, fainting or collapsing
and progressive abdominal
swelling. Although these signs
can signify the onset of heart
failure, they are also shared
with other conditions and
therefore testing is vital for
the diagnosis. In Schauzer the
disease is caused by a mutation
in the RBM20gene, In Welsh
Springer Spaniel it is caused by
a mutation in the PLN-gene,
whereas is Doberman it can be
caused by a mutation in the PDK4
gene, and / or mutation in the
TTN gene.
cost £48.00
each
more informatrion is
available on the following links:
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new
CNS Atrophy with Cerebellar Ataxia (CACA)
Our cooperation partner Prof. Tosso Leeb and his team from the University of Bern have identified a new genetic variant causing a neurological disease called CNS atrophy and cerebellar ataxia (CACA) in the breed Belgian Shepherd. Affected puppies show uncoordinated movements, intention tremor, short episodes of spastic fits, general elevated muscle tone and a reduced swallowing reflex. Moreover, affected puppies show less body weight increase as their unaffected littermates. First signs could be observed at the age of about 2 weeks. However, the severity of the signs are highly variable. Many affected puppies have to be euthanized a few weeks after the first signs whereas an affected dog with less intense symptoms has been reported to become up to 10 years old.
cost £48.00
each
more informatrion is
available on the following link:
CNS Atrophy with Cerebellar Ataxia (CACA)
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new
Macular Corneal Dystrophy ( MCD / CHST6 )
Macular Corneal Dystrophy (MCD) is an inherited eye disease affecting humans and dogs. The disease characterized by progressive diffuse cloudiness of the cornea and the presence of grayish-white spots in the superficial corneal stroma. The disease is caused by a mutation in the CHST6 gene which causes abnormal accumulation of complex carbohydrates called glycosaminoglycans in the cornea, mainly in the keratocytes and the corneal epithelium.
Clinical symptoms are usually seen in affected middle aged dogs, and include: Visual impairment, corneal cloudiness, grey-white spots of various sizes on the cornea, blood vessels maybe seen across the corneal surface, increased intensity of the corneal cloudiness and loss of visual acuity.
This mutation has only been reported in Labrador Retrievers, but may be found in Labrador-cross breeds.
Treatment: in dogs there is no treatment. In human, this is treated by corneal transplant.
The test
is part of the Kennel Club DNA
testing scheme in Labrador
Retriever
cost £48.00
each
more informatrion is
available on the following link:
Macular Corneal Dystrophy ( MCD / CHST6 )
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new
Ichthyosis Type 2
Ichthyosis type 2 is another variant which causes Ichthyosis in Golden Retriever, this test helps in explaining cases which was tested negative for the already known Ichrthyosis variant. Ichthyosis is a genetic disease causing dysfunction of the keratin in the skin, which leads to the production of large, differently pigmented skin scales. Due to the fish-like look of this scales the name was formed from the Greek word for fish: "Ichthys". Additionally, the pigmentation of the skin can be altered.
Dogs which are affected by this dermatosis develop first symptoms soon after birth. Unfortunately, there is no treatment for this disease. In some cases, formation of scales decreases in old dogs.
cost £48.00
each
more informatrion is
available on the following link:
Ichthyosis type 2 (ICH 2) in Golden Retriever
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Progressive Retinal Atrophy (PRA)
The following Progressive retinal atrophy (PRA) tests have recently been added:
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Pituitary Dwarfism
the test is now valid for the following breeds: Czechoslovakian Wolfdog, German Shepherd, Karelian Bear Dog, Lapland Reindeer Dog, Lapponian Herder, Saarloos Wolfdog, Tibetan Terrier, White Swiss Shepherd
Inherited Dwarfism is a condition in which the production of the Growth Hormone (GH) is inadequate. Growth hormone is secreted by the pituitary gland and has many effects on the body including control of growth rate, maintenance of hair coat, and bone and teeth development. Affected dogs appear normal at birth, but show evidence of failure to grow by two to three months of age. Symptoms include small stature compared to littermates, retention of puppy coat, hair loss, darkening of the skin, delayed eruption or absence of permanent teeth, a shrill bark, Small testicles and sometimes infertility in the male, Absence of heat and sometimes infertility in the female.
Affected dogs appear normal at birth, but show evidence of failure to grow by two to three months of age. Symptoms include small stature compared to littermates, retention of puppy coat, hair loss, darkening of the skin, delayed eruption or absence of permanent teeth, a shrill bark, Small testicles and sometimes infertility in the male, Absence of heat and sometimes infertility in the female.
The test is part of the
Kennel Club DNA testing scheme
in Tibetan Terrier
cost £48.00
each
more informatrion is
available on the following link:
Dwarfism (Pituitary Dwarfism / Hypopituitarism)
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new
Chihuahua DNA bundle
- Chondrodystrophy (CDDY with IVDD Risk) and Chondrodysplasia (CDPA)
- Macrothrombocytopenia ( MTC-D )
- Neuronal Ceroid Lipofuscinosis ( CL / NCL )
- Progressive Retinal Atrophy (prcd-PRA): (8094P / 8127)
cost £138.00
each
more informatrion is
available on the following link:
Chihuahua DNA bundle
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new
Giant Schnauzer DNA bundle
- Degenerative Myelopathy / Degenerative Radiculomyelopathy) DM (Exon 2)
- Dilated Cardiomyopathy ( DCM )
- Hyperuricosuria / Urate Stones (HUU, SLC)
- NECAP-1 Progressive Retinal Atrophy ( NECAP1 PRA / NECAP PRA5)
KC* DNA scheme in Giant Schnauzer
- Progressive Retinal Atrophy (prcd-PRA): (8094P / 8127)
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new
Russian Black Terrier DNA bundle
- Degenerative Myelopathy / Degenerative Radiculomyelopathy) DM (Exon 2)
- Hyperuricosuria / Urate Stones (HUU, SLC)
KC* DNA scheme in Russian Black Terrier (RBT)
- Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP)
KC* DNA scheme in Russian Black Terrier (RBT)
cost £138.00
more informatrion is
available on the following link:
Russian Black Terrier DNA bundle
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new
Yorkshire Terrier DNA bundle
- Chondrodystrophy (CDDY with IVDD Risk)and Chondrodysplasia (CDPA)
- L-2-HGA ( L- 2 - hydroxyglutaric aciduria ) L2HGA
- Primary Lens Luxation (PLL)
- Progressive Retinal Atrophy (prcd-PRA): (8094P / 8127)
- Subacute Necrotizing Encephalopathy (SNE)
cost £156.00
more informatrion is
available on the following link:
Yorkshire Terrier DNA bundle
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new
Bulldog DNA bundle
- Degenerative Myelopathy / Degenerative Radiculomyelopathy) DM (Exon 2)
- Hyperuricosuria / Urate Stones (HUU, SLC)
KC* DNA scheme in Bulldog (English)
- Cystinuria type III
- Canine Multi-Focal Retinopathy (CMR)
cost £138.00
more informatrion is
available on the following link:
Bulldog DNA bundle
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new
Tibetan Terrier DNA bundle
- Neuronal Ceroid Lipofuscinosis ( CL / NCL )
KC* DNA scheme in Tibetan Terrier
- Primary Lens Luxation (PLL)
KC* DNA scheme in Tibetan Terrier
- Progressive retinal atrophy ( rcd4-PRA) / LOPRA
KC* DNA scheme in Tibetan Terrier
- Degenerative Myelopathy / Degenerative Radiculomyelopathy) DM (Exon 2)
- Dwarfism (Pituitary Dwarfism / Hypopituitarism)
KC* DNA scheme in Tibetan Terrier
cost £156.00
more informatrion is
available on the following link:
Tibetan Terrier DNA bundle
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new
Irish Red & White Setter DNA bundle
- CLAD (Canine Leukocyte Adhesion Deficiency)
- Globoid Cell Leukodystrophy (Krabbe Disease)
- von Willebrand disease Type I (vWD I)
KC* DNA scheme in Irish Red and White Setter
- Progressive Retinal Atrophy (rcd1 PRA)
- Progressive retinal atrophy ( rcd4-PRA) / LOPRA
cost £138.00
more informatrion is
available on the following link:
Irish Red & White Setter DNA bundle
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new
Labradoodle DNA bundle
- Degenerative Myelopathy / Degenerative Radiculomyelopathy) DM (Exon 2)
- Exercise Induced Collapse ( EIC )
- Hereditary Nasal Parakeratosis (HNPK)
- Dwarfism (Skeletal Dysplasia 2 / SD2 )
- Neonatal encephalopathy (NE / NEWS)
- von Willebrand disease Type I (vWD I)
- Hereditary Myopathy / Centronuclear Myopathy (HMLR, CNM)
- Progressive Retinal Atrophy (prcd-PRA): (8094P / 8127)
- Progressive retinal atrophy ( rcd4-PRA) / LOPRA
cost £240.00
more informatrion is
available on the following link:
Labradoodle DNA bundle
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new Kennel Club DNA testing schemes
The following tests are now part of the Kennel Club DNA testing schemes:
- Stargardts disease (STGD) in Labrador Retriever
more ..
- Macular Corneal Dystrophy (MCD) in Labrador Retriever
more ..
- X-linked PRA Type 1 (XL-PRA1) in Samoyed more ..
- Hereditary Nephritis / X-linked (XLHN) in Samoyed
more ..
- Copper Toxicosis (COMMD1) in Bedlington Terrier
more ..
- Pituitary Dwarfism in Tibetan Terrier
more ..
- Leukoencephalomyelopath (LEMP) in Rottweiler
more ..
- Raine?s syndrome/ Dental hypomineralisation in Border Collie
more ..
- Amelogenesis Imperfecta / Familial Enamel Hypoplasia (AI/FEH) in Japanese Akita Inu
more ..
- PRA (prcd-PRA) in American Cocker Spaniel and Barbet
more ..
- CNGA1 - PRA in Shetland Sheepdog
more ..
- vWD type 1 in Papillon (Continental Toy Spaniel)
more ..
- Primary Open Angle Glaucoma (POAG) in Norwegian Elkhound
more ..
- Dwarfism (Chondrodysplasia / disproportinate short-limbed) in Norwegian Elkhound.
more ..
- NECAP1 PRA / NECAP PRA5 in Giant Schnauzer
more ..
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testing is easy
To test a dog, we need a DNA sample, which can be collected using simple mouth swabs or a blood sample collected by the vet. Both buccal swabs and blood tubes are available from us free of charge. Samples can be sent to our Manchester address below.
Turnaround 2-3 weeks or sooner for most DNA test.
Request Sample Materials
LABOKLIN is a DIN EN ISO / IEC 17025 Accredited laboratory. This means that all our tests are performed according to the reliable accreditation standards and verified procedures.
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LABOKLIN
(UK),
125
Northenden
Road,
Manchester,
Greater
Manchester,
M33
3HF,
United
Kingdom
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