We are delighted to announce that LABOKLIN will be returning to Crufts from
5th to 8th March 2026, an event we always look forward to and one that gives us the chance to connect with so many breeders.
It is a pleasure meeting everyone, whether you are dropping off a sample, discussing a test, suggesting a new bundle, asking about coat colour inheritance, or simply stopping by to say hello.
We look forward to seeing you there.
Our stand is located in Hall 3 opposite the restaurant, it is stand number 3-46 as shown in the diagram.
Meet the team
We are pleased to announce that
our genetic expert Dr Christoph
Beiztinger will be at Crufts and
will be pleased to answer any
questions you may have.
We always talk on the phone, by email or even via facebook, however, at Crufts we are very excited to meet you in person,
it is a fantastic opportunity to talk through your testing needs and explore how we can support you. Please stop by and say hi.
Crufts offer
10% discount on all DNA tests submitted at Crufts !
and this offer includes our Breed Specific DNA Bundles, the brand new KC breed bundles and the new comprehensive XXL bundle.
How to submit a sample at Crufts :
Bring your dog to our stand 3-46: 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 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:
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 )
Payments can be made by card, cheque, cash, postal Order, bank transfer and paypal.
To calculate your Crufts 2026 price, simply take the standard catalogue price and apply 10%. You can simply multiply the catalogue price by 0.9. For example:
Catalogue price:£48.00 Crufts discounted price:£48.00 x 0.9=£43.20
try the following calculator:
Crufts discounted price (10% off): £0.00
Turnaround: 1-3 weeks for the majority of tests from Monday 9th March.
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
Unit 20, Wheel Forge Way
Trafford Park
Manchester
M17 1EH
Dermoid Sinus is a serious congenital condition primarily seen in Rhodesian Ridgebacks, although it can occasionally affect other breeds. It is a tubular defect that arises during embryonic development when the skin and nervous system fail to completely separate. This results in 'noodle-like' tissue formations that abnormally connect the upper layers of the skin to deeper structures, such as muscles or even the spinal cord.
Detecting Dermoid Sinus can be particularly challenging, even for experienced veterinarians, as the condition is not always visible externally and may require careful examination or imaging to identify. If left untreated, the sinus can lead to complications such as infections, abscesses, and pain, significantly affecting the dog's health and quality of life.
Dogs affected by Dermoid Sinus, including those that have undergone surgical removal of the condition, have traditionally been excluded from breeding programs to prevent passing the condition on to their offspring, as it is highly heritable. However, with the introduction of a new DNA test for Dermoid Sinus, breeders now have the ability to make informed breeding decisions by ensuring that new born puppies are not at high risk of developing Dermoid Sinus.
cost £66.00
more information is available on the following link:
The Rhodesian Ridgeback is distinguished by a dorsal ridge of hair that grows in the opposite direction to the rest of the coat. This ridge is associated with a genetic variant on chromosome 18. Genetic testing can determine whether the ridge allele is present in heterozygous form (R/r) or homozygous form (R/R). By assessing the genotypes of breeding partners, it is possible to estimate the likelihood of ridgeless offspring
A defining characteristic of the Rhodesian Ridgeback is the ridge: a clearly demarcated strip of hair along the spine that grows forward, opposite to the surrounding coat. Breed standards specify that the ridge should begin immediately behind the shoulders and extend centrally along the back to approximately the level of the hip bones, tapering slightly towards the rear. Ideally, the ridge measures 4 -5 cm in width at the shoulder region and is sharply distinguishable from the adjacent coat. Within the ridge, two hair whorls (crowns) are typically present, positioned opposite one another in a symmetrical, mirror-image arrangement.
cost 66.00
more information is available on the following link:
Degenerative Encephalopathy (DE) is a progressive hereditary neurological disorder in Nova Scotia Duck Tolling Retrievers. Affected dogs may show sleep-related involuntary movements, cognitive decline, anxiety, and worsening neurological signs over time. A risk variant in the RB1CC1 gene has been linked to the disease, and genetic testing helps identify carriers and supports informed breeding and clinical decisions. This test is part of the Official UK Kennel Club DNA Testing Scheme.
cost 48.00
more information is available on the following link:
A variant in the CAD gene has been linked to epileptic encephalopathy in
Bengal cats. Affected kittens may show symptoms from around three months of age,
including clusters of generalised tonic seizures, abnormal behaviour, and reduced responsiveness.
Seizures often occur during sleep and can involve sudden jumping, increased muscle tone, facial twitching, chewing
movements, salivation, and brief disorientation afterwards.
Affected kittens may also appear unusually quiet, show episodes of obtundation or agitation, and
display neurological abnormalities such as an absent menace response. The CAD gene
is essential for pyrimidine synthesis and several metabolic pathways, and dysfunction can lead to severe
neurological impairment. As the condition responded only partially to treatment, euthanasia was chosen due to
poor quality of life.
cost 48.00
more information is available on the following link:
Progressive Retinal Atrophies (PRA) are inherited diseases that cause retinal degeneration and vision loss, with many forms being breed-specific. Typical clinical signs include tapetal hyper-reflectivity and retinal vascular attenuation. Genetic testing helps identify affected dogs before symptoms or breeding. In Labrador Retrievers, a variant in the GTPBP2 gene is linked to PRA, leading to progressive visual decline. Affected dogs may stop responding to visual cues and rely more on smell. Onset usually occurs between 7 months and 1.5 years, and a secondary cataract may develop as the disease progresses.
cost 48.00
more information is available on the following link:
A genetic form of polioencephalopathy in Eurasier dogs is linked to a variant in the
MECR gene. Affected puppies typically show signs between 2 and 6 months, including
ataxia, hypermetric gait, dystonia, and sudden limb flexion or extension,
often triggered by excitement or noise. Additional features may include muscle atrophy,
abnormal posture, and divergent strabismus, though behaviour and awareness remain normal.
The MECR gene is essential for mitochondrial energy metabolism, and variants can cause
neurodegenerative changes. This DNA test helps identify carriers and affected dogs early, supporting informed
breeding decisions. Trait of inheritance: autosomal recessive.
cost 48.00
more information is available on the following link:
Basset Hounds can suffer from a glycogen storage disease (GSD) caused by a genetic variant in the RBCK1 gene. This autosomal recessive disorder leads to abnormal glycogen accumulation. Clinical signs typically begin between 8 and 12 months of age with chronic vomiting and diarrhea. As the disease progresses, affected dogs may develop muscle weakness, cardiac complications, and an increased risk of sudden cardiac death
cost 48.00
more information is available on the following link:
Cerebellar Abiotrophy (CA) is an inherited neurological disorder in
Australian Kelpies, causing progressive loss of coordination and balance due to
degeneration of cerebellar nerve cells. Affected dogs may show unsteady gait,
poor coordination, head tremors, and worsening motor control.
Two genetic risk markers, VMP1 and LINGO3, are associated with CA,
both inherited in an autosomal recessive manner (with variable penetrance for LINGO3).
Genetic testing helps identify carriers and at-risk dogs, supporting responsible breeding
and long-term breed health.
cost 48.00
more information is available on the following link:
Hypertrophic Cardiomyopathy (HCM) is a heart muscle disease in
Golden Retrievers where the heart walls thicken, reducing the heart's ability to pump
effectively and increasing the risk of serious complications. Signs may include
cost 48.00
more information is available on the following link:
Primary Hyperparathyroidism (PHPT) is an inherited disorder in
Keeshonds and German Spitz where the parathyroid glands produce excess hormone,
leading to persistently high calcium levels. Affected dogs may show
increased thirst and urination, weakness, vomiting,
weight loss, or kidney complications, often appearing later in life.
The condition is caused by a dominant genetic variant, meaning only one copy is needed to increase risk.
Genetic testing helps identify affected dogs early, guide breeding decisions, and support long-term health monitoring.
This test is part of the Official UK Kennel Club DNA Testing Scheme in Keeshond.
cost 48.00
more information is available on the following link:
26th April 2026 at the Exhibition Centre Liverpool L3 4FP
We are delighted to announce that Laboklin will be exhibiting at the Supreme Cat Show 2026.
This year's show will take place on 26th April 2026 at the Exhibition Centre Liverpool and forms
part of the prestigious World Cat Congress, held from 23-27 April 2026.
We look forward to meeting breeders, exhibitors, and cat enthusiasts throughout this landmark international event.
As a special show offer, we are pleased to provide a 10% discount on all samples submitted at our stand on the day.
We hope to see you there for what promises to be an exceptional celebration of the global cat community.
more information will be published on the Laboklin website and our facebook page soon.
new
DLA Typing: Autoimmune Risks
in all breeds
Dog Leukocyte Antigen (DLA) typing provides valuable insight into a dog's
immune system genetics and helps assess the level of genetic diversity within its immune response.
DLA genes are inherited in fixed combinations known as haplotypes, and maintaining diversity in these
genes supports stronger, more resilient immune function. Certain haplotypes are associated with higher or lower risk of
autoimmune conditions such as diabetes mellitus, exocrine pancreatic insufficiency,
hypothyroidism and Addison's disease. DLA typing identifies which haplotypes a dog carries,
showing whether they are heterozygous (diverse) or homozygous (uniform). This information helps
breeders choose compatible mates, act responsibly, and reduce long-term health risks within the population. An
EDTA blood sample or a special optimised swab is required for this test.
cost 120.00
more information is available on the following link:
We are excited to introduce a new DNA test for Feline Atherosclerosis.
Atherosclerosis is a chronic inflammatory vascular disease caused by the accumulation of
LDL-derived cholesterol on arterial walls. While common in humans, it is rare in animals.
Recent research has identified spontaneous cases in Korat cats, characterised by severe
hypercholesterolemia and clinical signs of congestive heart failure, with
histopathological features similar to human atherosclerosis.
Our new test targets the specific genetic variant associated with this condition, providing
valuable insights for breeders, veterinarians, and researchers. Early identification helps guide
breeding decisions, support health monitoring, and reduce the risk of
producing affected cats.
cost 48.00
more information is available on the following link:
Hypertrophic cardiomyopathy (HCM) is one of the most common heart diseases in cats,
and many affected cats are treated with clopidogrel to reduce the risk of dangerous blood clots.
Recent research has shown that some cats carry a variant in the P2RY1 gene that can make
clopidogrel less effective. Our new genetic test identifies whether a cat carries this variant,
helping veterinarians tailor treatment more accurately.
In cats with this variant, clinicians may consider alternative or additional thromboprophylactic therapy
to ensure optimal protection against clot-related complications.
cost 48.00
more information is available on the following link:
GSD Breed Council Premium DNA Profiling & Parentage Verification
new partnership
A new partnership between Laboklin, the German Shepherd Dog Breed Council (GSDBC), and the German Shepherd Dog League of Great Britain (GSDL) now provides a dedicated Premium DNA Profiling and Parentage Verification service for German Shepherds. This programme ensures accurate parentage records through a secure database managed by Laboklin and supports responsible breeding using advanced SNP-based genetic analysis.
Breeders submit a EDTA blood sample using the official GSDBC form, allowing Laboklin to store each dog's DNA profile for future verification. Participants receive an ISAG 2020-standard DNA profile, a detailed report including genetic diversity metrics, official entry into the GSDBC survey database, parentage verification (where parental profile(s) exist), and a genetic variability report to help guide informed breeding decisions.
Parentage is verified by comparing a dog's DNA profile against potential parents already stored in the
GSDBC database. The submitter does not need to provide details of the sire or dam - the system
automatically detects one or both parents as long as their SNP DNA profile(s) are already in the database.
Successful matches depend on prior submissions.
more information is
available on the following link:
Primary Hyperparathyroidism (PHPT) in Keeshond
more ..
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.
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),
Unit 20, Wheel Forge Way, Trafford Park
Manchester,
Greater
Manchester,
M17
1EH,
United
Kingdom
