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DICER1 FISH Probe

The DICER1 FISH probe is designed to hybridize to the DICER1 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
DICER1-20-OR  (Standard Design) 20 (40 μL) 200 μL
DICER1-20-RE 20 (40 μL) 200 μL
DICER1-20-GO 20 (40 μL) 200 μL
DICER1-20-GR 20 (40 μL) 200 μL
DICER1-20-AQ 20 (40 μL) 200 μL
DICER1-20-DIG 20 (40 μL) 200 μL
DICER1-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene encodes a protein possessing an RNA helicase motif containing a DEXH box in its amino terminus and an RNA motif in the carboxy terminus. The encoded protein functions as a ribonuclease and is required by the RNA interference and small temporal RNA (stRNA) pathways to produce the active small RNA component that represses gene expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]

Gene Details

Gene Symbol: DICER1

Gene Name: Dicer 1, Ribonuclease III

Chromosome: CHR14: 95552564-95623759

Locus: 14q32.13

Gene Diseases

The DICER1 gene has been associated with the following diseases:

Disease Name
2-Hydroxyglutaricaciduria
49,XXXXX Syndrome
Aagenaes Syndrome
Abderhalden-Kaufmann-Lignac Syndrome
Abrikosov's Tumor
Achard Syndrome
Achard-Thiers Syndrome
Acrocephalopolysyndactyly Type II
Acrootoocular Syndrome
Acrorenal Syndrome
Adenocarcinoid Tumor
Adenocarcinoma
Akaba Hayasaka Syndrome
Akesson Syndrome
Aksu Von Stockhausen Syndrome
Aloi Tomasini Isaia Syndrome
Alsing Syndrome
Ameloonychohypohidrotic Syndrome
Androblastoma Of Ovary
Angiolipomatosis, Familial
Ansell Bywaters Elderking Syndrome
Arakawa Syndrome 2
AREDYLD Syndrome
Arima Syndrome
Atherosclerosis
Athrombia, Essential
Atrophy
Aughton Syndrome
Ayazi Syndrome
Azoospermia
BADS Syndrome
Baetz-Greenwalt Syndrome
Bagatelle Cassidy Syndrome
Bangstad Syndrome
Bankart Lesions
Banki Syndrome
Banti's Syndrome
Basaran Yilmaz Syndrome
Bassoe Syndrome
Bazopoulou Kyrkanidou Syndrome
Beardwell Syndrome
Beemer Ertbruggen Syndrome
Bellini Chiumello Rimoldi Syndrome
Biemond Syndrome II
Blepharo-cheilo-dontic Syndrome
Blount Disease
Body Remains
Boerhaave Syndrome
Bone Anteversion
Bone Retroversion
Bonneau Syndrome
Boudhina Yedes Khiari Syndrome
Brachioskeletogenital Syndrome
Brachymesomelia Renal Syndrome
Brachymesophalangy 2 And 5
Breast Cancer, Familial
Breast Cancer, Familial Male
Broad-Betalipoproteinemia
Brunoni Syndrome
CAHMR Syndrome
Calabro Syndrome
CAMFAK Syndrome
Campomelia Cumming Type
Cancer
Cancer Of The Oviduct
CANOMAD Syndrome
Cantalamessa Baldini Ambrosi Syndrome
Carcinogenesis
Carcinoma
Cardiocranial Syndrome
Carrington Syndrome
CATSHL Syndrome
CD8 Deficiency, Familial
Cerebelloparenchymal Disorder II
Cerebelloparenchymal Disorder VI
Cerebrooculonasal Syndrome
Chilaiditi Syndrome
CLAPO Syndrome
Cleidorhizomelic Syndrome
Collagenoma, Familial Cutaneous
COMPLEMENT COMPONENT 2 DEFICIENCY
Complement Component 4, Partial Deficiency Of
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
Contrecoup Injury
Corneodermatoosseous Syndrome
Coxoauricular Syndrome
Cranioacrofacial Syndrome
Craniofaciofrontodigital Syndrome
Craniomicromelic Syndrome
Crome Syndrome
Cryofibrinogenemia, Familial Primary
Cryptotia, Familial
Curatolo Cilio Pessagno Syndrome
Cystic Disease Of Lung
D-glycericacidemia
Daentl Towsend Siegel Syndrome
Daish Hardman Lamont Syndrome
Daneman Davy Mancer Syndrome
Davenport Donlan Syndrome
Death
Dermatoosteolysis Kirghizian Type
Devriendt Syndrome
Dieterich's Disease
Digitorenocerebral Syndrome
Dimauro Disease
Disease
Drachtman Weinblatt Sitarz Syndrome
Faciocardiomelic Syndrome
Faciocardiorenal Syndrome
Fairbank Disease
Familial Dermographism
Familial Hyperbeta- And Prebetalipoproteinemia
Familial Primary Gastric Lymphoma
Familial Streblodactyly
Familial Wilms Tumor 2
Fatty Liver
Fever
Fibrosis
FLOTCH Syndrome
Flynn Aird Syndrome
Fountain Syndrome
Fragile X Syndrome
Franceschini Vardeu Guala Syndrome
Freiberg's Disease
Frontoocular Syndrome
Furlong Syndrome
Furukawa Takagi Nakao Syndrome
Gastric Sneezing
Gastrocutaneous Syndrome
Gemignani Syndrome
GEMSS Syndrome
Genoa Syndrome
Giacheti Syndrome
Gigantiform Cementoma, Familial
Glioma
Glioma Of Brain, Familial
Goiter
Goiter, Multinodular 2
Goiter, Multinodular 3
Gollop Coates Syndrome
GOMBO Syndrome
Granddad Syndrome
Granulosa Cell Tumor
Grover's Disease
Grubben De Cock Borghgraef Syndrome
Gurrieri Sammito Bellussi Syndrome
Hadziselimovic Syndrome
Hagemoser Weinstein Bresnick Syndrome
Halal Syndrome
Hamanishi Ueba Tsuji Syndrome
Hamano Tsukamoto Syndrome
Hamartoma
Hapnes Boman Skeie Syndrome
Hardikar Syndrome
Hepatic Adenomas, Familial
Hepatitis
Hepatitis B
Hepatitis C
Herrmann Syndrome
Hersh Podruch Weisskopk Syndrome
Hooft Disease
Hordnes Engebretsen Knudtson Syndrome
Human Balantidiasis
Hunt's Syndrome
Hyperreninemic Hypoaldosteronism, Familial, 2
Hypoadrenocorticism, Familial
Hypoxia
Iida Kannari Syndrome
Infection
Infertility
Inflammation
Influenza, Human
Intestinal Helminthiasis
Jagell Holmgren Hofer Syndrome
Kaplowitz Bodurtha Syndrome
Karoshi Death
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
Langerhans Cell Sarcoma
Lelis Syndrome
Lemierre Syndrome
Leukemia
Leydig Cell Tumor
Lung Agenesis
Lymphoma
Lymphoma, Large B-Cell, Diffuse
Lymphoma, Primary Cutaneous Anaplastic Large Cell
Lyngstadaas Syndrome
Macular Degeneration
Macular Degeneration, Age-Related, 1
Macular Degeneration, Age-Related, 11
MACULAR DEGENERATION, AGE-RELATED, 12
MACULAR DEGENERATION, AGE-RELATED, 13
MACULAR DEGENERATION, AGE-RELATED, 14
MACULAR DEGENERATION, AGE-RELATED, 15
Macular Degeneration, Age-Related, 2
Macular Degeneration, Age-Related, 3
Macular Degeneration, Age-Related, 4
MACULAR DEGENERATION, AGE-RELATED, 5
Macular Degeneration, Age-Related, 6
Macular Degeneration, Age-Related, 7
MACULAR DEGENERATION, AGE-RELATED, 8
Macular Degeneration, Age-Related, 9
Malignant Fever
Malignant Mesenchymal Tumor
Malignant Teratocarcinosarcoma
Malouf Syndrome
Manouvrier Syndrome
Marchiafava-Bignami Disease
Marsden Syndrome
Massa Casaer Ceulemans Syndrome
May-Thurner Syndrome
Mehes Syndrome
Melanoma
Melanoma, Cutaneous Malignant
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 9
Melhem Fahl Syndrome
Mengel Konigsmark Syndrome
Meralgia Paraesthetica, Familial
Merlob Grunebaum Reisner Syndrome
Meyenburg-Altherr-Uehlinger Syndrome
Mirizzi Syndrome
Mollica Pavone Antener Syndrome
MOMES Syndrome
Mononen Karnes Senac Syndrome
Morgellons Disease
Multiple Chronic Conditions
Multiple Pulmonary Nodules
Multiple Sclerosis
Nasodigitoacoustic Syndrome
Nasopharyngeal Carcinoma
Nathalie Syndrome
Necrosis
Neoplasms
Neuroblastoma
Neurofaciodigitorenal Syndrome
Nevo Syndrome
Nicolau Syndrome
Nievergelt Syndrome
Nivelon Nivelon Mabille Syndrome
Non-alcoholic Fatty Liver Disease
Obesity
Oculoauriculofrontonasal Syndrome
Oculocerebrocutaneous Syndrome
Oculodental Syndrome Rutherfurd Syndrome
Oculootoradial Syndrome
Oculopalatocerebral Syndrome
Oculopalatoskeletal Syndrome
Oculorenocerebellar Syndrome
Oligosynaptic Infertility
Onat Syndrome
Opticocochleodentate Degeneration
Oroticaciduria 1
Oslam Syndrome
Otofacioosseous-Gonadal Syndrome
Otoonychoperoneal Syndrome
Pachydermodactyly, Familial
Paraphilic Disorders
Partial Agenesis Of Corpus Callosum
Pascual Castroviejo Syndrome
Pashayan Syndrome
Passovoy Factor
Pavone Fiumara Rizzo Syndrome
Pechet Factor Deficiency
PHACE Association
Pilotto Syndrome
Piriformis Muscle Syndrome
Pituitary Hormone Deficiency, Combined, 1
Pituitary Hormone Deficiency, Combined, 2
Pituitary Hormone Deficiency, Combined, 4
Piussan Lenaerts Mathieu Syndrome
Podder-Tolmie Syndrome
Polythelia, Familial
Postthrombotic Syndrome
Precancerous Conditions
Preeyasombat Varavithya Syndrome
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2
PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3
Pregnancy, Cornual
Prepapillary Vascular Loops
Primary Dysautonomias
Primary Release Disorder Of Platelets
Propping Zerres Syndrome
Prostate Cancer, Familial
Pseudoaminopterin Syndrome
Pseudoarylsulfatase A Deficiency
Pseudotrisomy 13 Syndrome
Qazi Markouizos Syndrome
Rambaud Galian Syndrome
Ramer Ladda Syndrome
Recurrence
Reginato Schiapachasse Syndrome
Renal Aminoacidurias
Retinohepatoendocrinologic Syndrome
Rhabdomyosarcoma
RHYNS Syndrome
Ribbing Disease
Richards-Rundle Syndrome
Rombo Syndrome
Rosselli-Gulienetti Syndrome
Rudiger Syndrome
Sakoda Complex
Salcedo Syndrome
Sammartino De Crecchio Syndrome
Sandifer Syndrome
Sarcoma
Sarcoma, Myeloid
Satoyoshi Syndrome
Schlegelberger Grote Syndrome
Schofer Beetz Bohl Syndrome
Scholte Syndrome
Schrander-Stumpel Theunissen Hulsmans Syndrome
Sclerosis
Seaver Cassidy Syndrome
Seemanova Lesny Syndrome
Sener Syndrome
Sex Cord-Gonadal Stromal Tumors
Shapiro Syndrome
Silengo Lerone Pelizza Syndrome
Sillence Syndrome
Sohval Soffer Syndrome
Steinfeld Syndrome
Summitt Syndrome
SUNCT Syndrome
SUPPRESSOR OF TUMORIGENICITY 3
Susac Syndrome
Syndrome
Syringomas, Multiple
Tabatznik Syndrome
Tatsumi Factor Deficiency
Thyrocerebral-retinal Syndrome
Thyroid Cancer, Follicular
Tonoki Syndrome
Translocation, Genetic
Trichodental Syndrome
Triple X Syndrome
Trueb Burg Bottani Syndrome
Tsukahara Syndrome
Tucker Syndrome
Upington Disease
Uterine Retroversion
Velofacioskeletal Syndrome
Verloove-Vanhorick Brubakk Syndrome
Volcke Soekarman Syndrome
Walbaum Titran Durieux Crepin Syndrome
Waldmann Disease
Warburton Anyane Yeboa Syndrome
Warman Mulliken Hayward Syndrome
Weismann Netter Syndrome
Wilms Tumor
WILMS TUMOR 5
WILMS TUMOR 6
Wyburn Mason's Syndrome
Young McKeever Squier Syndrome
Young 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: DICER1 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: DICER1-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping