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BBS10 FISH Probe

The BBS10 FISH probe is designed to hybridize to the BBS10 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.

SKU Test Kits Buffer Dye Color Order Now
BBS10-20-OR  (Standard Design) 20 (40 μL) 200 μL
BBS10-20-RE 20 (40 μL) 200 μL
BBS10-20-GO 20 (40 μL) 200 μL
BBS10-20-GR 20 (40 μL) 200 μL
BBS10-20-AQ 20 (40 μL) 200 μL
BBS10-20-DIG 20 (40 μL) 200 μL
BBS10-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10. [provided by RefSeq, Jan 2010]

Gene Details

Gene Symbol: BBS10

Gene Name: Bardet-Biedl Syndrome 10

Chromosome: CHR12: 76738265-76742222

Locus: 12q21.2

Gene Diseases

The BBS10 gene has been associated with the following diseases:

Disease Name
2-Hydroxyglutaricaciduria
49,XXXXX Syndrome
Aagenaes Syndrome
Abderhalden-Kaufmann-Lignac Syndrome
Achard Syndrome
Achard-Thiers Syndrome
Acrocephalopolysyndactyly Type II
Acrootoocular Syndrome
Acrorenal Syndrome
Acrorenal Syndrome Recessive
Akaba Hayasaka Syndrome
Akesson Syndrome
Aloi Tomasini Isaia Syndrome
Alsing Syndrome
Ameloonychohypohidrotic Syndrome
Androblastoma Of Ovary
Ansell Bywaters Elderking Syndrome
Arakawa Syndrome 2
AREDYLD Syndrome
Arima Syndrome
Aughton Syndrome
Ayazi Syndrome
BADS Syndrome
Baetz-Greenwalt Syndrome
Bagatelle Cassidy Syndrome
Bangstad Syndrome
Banki Syndrome
Banti's Syndrome
Bardet-Biedl Syndrome
Bardet-Biedl Syndrome 11
Bardet-Biedl Syndrome 13
Bardet-Biedl Syndrome 14
BARDET-BIEDL SYNDROME 15
BARDET-BIEDL SYNDROME 16
BARDET-BIEDL SYNDROME 17
BARDET-BIEDL SYNDROME 18
BARDET-BIEDL SYNDROME 19
BARDET-BIEDL SYNDROME 20
BARDET-BIEDL SYNDROME 21
Basaran Yilmaz Syndrome
Bassoe Syndrome
Bazopoulou Kyrkanidou Syndrome
Beardwell Syndrome
Beemer Ertbruggen Syndrome
Bellini Chiumello Rimoldi Syndrome
Biemond Syndrome II
Birth Weight
Blepharo-cheilo-dontic Syndrome
Blindness
Blount Disease
Boerhaave Syndrome
Bonneau Syndrome
Boudhina Yedes Khiari Syndrome
Brachioskeletogenital Syndrome
Brachymesomelia Renal Syndrome
Brachymesophalangy 2 And 5
Brunoni Syndrome
CAHMR Syndrome
Calabro Syndrome
CAMFAK Syndrome
Campomelia Cumming Type
CANOMAD Syndrome
Cantalamessa Baldini Ambrosi Syndrome
Cardiocranial Syndrome
Carrington Syndrome
CATSHL Syndrome
Cerebelloparenchymal Disorder II
Cerebrooculonasal Syndrome
Chilaiditi Syndrome
CLAPO Syndrome
Cleidorhizomelic Syndrome
Cone Dystrophy 4
Corneodermatoosseous Syndrome
Coxoauricular Syndrome
Cranioacrofacial Syndrome
Craniofaciofrontodigital Syndrome
Craniomicromelic Syndrome
Crome Syndrome
Curatolo Cilio Pessagno Syndrome
Cysts
Daentl Towsend Siegel Syndrome
Daish Hardman Lamont Syndrome
Daneman Davy Mancer Syndrome
Davenport Donlan Syndrome
Dermatoosteolysis Kirghizian Type
Devriendt Syndrome
Dieterich's Disease
Digitorenocerebral Syndrome
Dimauro Disease
Disease
Drachtman Weinblatt Sitarz Syndrome
Faciocardiomelic Syndrome
Faciocardiorenal Syndrome
Fairbank Disease
FLOTCH Syndrome
Flynn Aird Syndrome
Fountain Syndrome
Franceschini Vardeu Guala Syndrome
Freiberg's Disease
Frontoocular Syndrome
Furlong Syndrome
Furukawa Takagi Nakao Syndrome
Gastrocutaneous Syndrome
Gemignani Syndrome
GEMSS Syndrome
Genoa Syndrome
Giacheti Syndrome
Gollop Coates Syndrome
GOMBO Syndrome
Granddad Syndrome
Grover's Disease
Gurrieri Sammito Bellussi Syndrome
Hadziselimovic Syndrome
Hagemoser Weinstein Bresnick Syndrome
Halal Syndrome
Hamanishi Ueba Tsuji Syndrome
Hamano Tsukamoto Syndrome
Hapnes Boman Skeie Syndrome
Hardikar Syndrome
HEART AND BRAIN MALFORMATION SYNDROME
Herrmann Syndrome
Hersh Podruch Weisskopk Syndrome
Hooft Disease
Hordnes Engebretsen Knudtson Syndrome
Human Balantidiasis
Hunt's Syndrome
Hypogonadism
Iida Kannari Syndrome
Jagell Holmgren Hofer Syndrome
Kaplowitz Bodurtha Syndrome
Kasabach-Merritt Syndrome
Kashani Strom Utley Syndrome
Katsantoni Papadakou Lagoyanni Syndrome
Kennerknecht Sorgo Oberhoffer Syndrome
Kleeblattschaedel Syndrome
Koone Rizzo Elias Syndrome
Kosztolanyi Syndrome
Krasnow Qazi Syndrome
Kuskokwim Disease
Kuzniecky Syndrome
Kyrle Disease
Lachiewicz Sibley Syndrome
Lacrimoauriculodentodigital Syndrome
Lambotte Syndrome
Lelis Syndrome
Lemierre Syndrome
Lyngstadaas Syndrome
Malouf Syndrome
Manouvrier Syndrome
Marchiafava-Bignami Disease
Marsden Syndrome
Massa Casaer Ceulemans Syndrome
May-Thurner Syndrome
Mehes Syndrome
Melhem Fahl Syndrome
Mengel Konigsmark Syndrome
Merlob Grunebaum Reisner Syndrome
Meyenburg-Altherr-Uehlinger Syndrome
Mirizzi Syndrome
Mollica Pavone Antener Syndrome
MOMES Syndrome
Mononen Karnes Senac Syndrome
Morgellons Disease
Nasodigitoacoustic Syndrome
Nathalie Syndrome
Neurofaciodigitorenal Syndrome
Nevo Syndrome
Nicolau Syndrome
Nievergelt Syndrome
Night Blindness
Nivelon Nivelon Mabille Syndrome
Obesity
Oculoauriculofrontonasal Syndrome
Oculocerebrocutaneous Syndrome
Oculodental Syndrome Rutherfurd Syndrome
Oculootoradial Syndrome
Oculopalatocerebral Syndrome
Oculopalatoskeletal Syndrome
Oculorenocerebellar Syndrome
Onat Syndrome
Opticocochleodentate Degeneration
Oroticaciduria 1
Oslam Syndrome
Otoonychoperoneal Syndrome
Pascual Castroviejo Syndrome
Pashayan Syndrome
Passovoy Factor
Pavone Fiumara Rizzo Syndrome
Pilotto Syndrome
Piussan Lenaerts Mathieu Syndrome
Podder-Tolmie Syndrome
Polydactyly
Polydactyly, Postaxial
Postthrombotic Syndrome
Preeyasombat Varavithya Syndrome
Pregnancy, Cornual
Primary Dysautonomias
Propping Zerres Syndrome
Pseudoaminopterin Syndrome
Pseudotrisomy 13 Syndrome
Qazi Markouizos Syndrome
Rambaud Galian Syndrome
Ramer Ladda Syndrome
Reginato Schiapachasse Syndrome
Renal Aminoacidurias
Retinal Cone Dystrophy 2
Retinal Cone Dystrophy 4
Retinal Degeneration
RETINAL DYSTROPHY AND OBESITY
Retinohepatoendocrinologic Syndrome
RHYNS Syndrome
Ribbing Disease
Richards-Rundle Syndrome
Rombo Syndrome
Rosselli-Gulienetti Syndrome
Rudiger Syndrome
Sakoda Complex
Salcedo Syndrome
Sandifer Syndrome
Satoyoshi Syndrome
Schlegelberger Grote Syndrome
Schofer Beetz Bohl Syndrome
Scholte Syndrome
Schrander-Stumpel Theunissen Hulsmans Syndrome
Seaver Cassidy Syndrome
Seemanova Lesny Syndrome
Sener Syndrome
Shapiro Syndrome
Silengo Lerone Pelizza Syndrome
Sillence Syndrome
Sohval Soffer Syndrome
Steinfeld Syndrome
Summitt Syndrome
SUNCT Syndrome
Susac Syndrome
Syndrome
Tabatznik Syndrome
Thyrocerebral-retinal Syndrome
Tonoki Syndrome
Trichodental Syndrome
Trueb Burg Bottani Syndrome
Tsukahara Syndrome
Tucker Syndrome
Upington Disease
Velofacioskeletal Syndrome
Verloove-Vanhorick Brubakk Syndrome
Volcke Soekarman Syndrome
Walbaum Titran Durieux Crepin Syndrome
Waldmann Disease
Warburton Anyane Yeboa Syndrome
Warman Mulliken Hayward Syndrome
Weight Gain
Weismann Netter Syndrome
Wyburn Mason's Syndrome
Yusho Disease
Zazam Sheriff Phillips Syndrome
Zechi-Ceide Syndrome
Zlotogora-Ogur Syndrome
Zuska's Disease

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Scientific Citations

There are currently no FISH related citations for this gene.

Product Details

Product: BBS10 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: BBS10-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping