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ATM FISH Probe

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

Gene Summary

The protein encoded by this gene belongs to the PI3/PI4-kinase family. This protein is an important cell cycle checkpoint kinase that phosphorylates; thus, it functions as a regulator of a wide variety of downstream proteins, including tumor suppressor proteins p53 and BRCA1, checkpoint kinase CHK2, checkpoint proteins RAD17 and RAD9, and DNA repair protein NBS1. This protein and the closely related kinase ATR are thought to be master controllers of cell cycle checkpoint signaling pathways that are required for cell response to DNA damage and for genome stability. Mutations in this gene are associated with ataxia telangiectasia, an autosomal recessive disorder. [provided by RefSeq, Aug 2010]

Gene Details

Gene Symbol: ATM

Gene Name: ATM Serine/threonine Kinase

Chromosome: CHR11: 108093558-108239826

Locus: 11q22.3

Gene Diseases

The ATM gene has been associated with the following diseases:

Disease Name
2-Hydroxyglutaricaciduria
49,XXXXX Syndrome
Aagenaes Syndrome
Abc Disease
Abderhalden-Kaufmann-Lignac Syndrome
Abrikosov's Tumor
Achard Syndrome
Achard-Thiers Syndrome
Acquired Hypoprothrombinemia
Acrocephalopolysyndactyly Type II
Acrokeratoderma, Hereditary Papulotranslucent
Acrootoocular Syndrome
Acrorenal Syndrome
Acrorenal Syndrome Recessive
Acute Retroviral Syndrome
Adenocarcinoid Tumor
Adenocarcinoma
Adenoma
Adrenocortical Adenoma
Adrenocortical Carcinoma
Adrenocortical Carcinoma, Hereditary
Akaba Hayasaka Syndrome
Akesson Syndrome
Aloi Tomasini Isaia Syndrome
Alsing Syndrome
Ameloonychohypohidrotic Syndrome
Androblastoma Of Ovary
Anemia
Angioedemas, Hereditary
Angiolipomatosis, Familial
Ansell Bywaters Elderking Syndrome
Arakawa Syndrome 2
AREDYLD Syndrome
Arima Syndrome
Arrhenoblastoma--Thyroid Adenoma
Arthritis
Astrocytoma
Asymptomatic Diseases
Ataxia
Ataxia Telangiectasia
Ataxia-Telangiectasia Variant
Athrombia, Essential
Atrophy
Aughton Syndrome
Ayazi Syndrome
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
Bloom Syndrome
Blount Disease
Boerhaave Syndrome
Bone Anteversion
Bone Retroversion
Bonneau Syndrome
Boudhina Yedes Khiari Syndrome
Brachioskeletogenital Syndrome
Brachymesophalangy 2 And 5
Breast Cancer, Familial
Breast Cancer, Familial Male
Breast Neoplasms
Brunoni Syndrome
CAHMR Syndrome
Calabro Syndrome
CAMFAK Syndrome
Campomelia Cumming Type
Cancer
CANOMAD Syndrome
Cantalamessa Baldini Ambrosi Syndrome
Car Factor Deficiency
Carcinogenesis
Carcinoma
Cardiocranial Syndrome
Carrington Syndrome
CATSHL Syndrome
Cerebellar Ataxia
Cerebelloparenchymal Disorder II
Cerebrooculonasal Syndrome
Cervical Dystonia, Primary
Chilaiditi Syndrome
Childhood Myocerebrohepatopathy Spectrum
Cholangitis
Chromosomal Instability
Chromosome 11q Partial Deletion
Chromosome 11q Trisomy
Chromosome Aberrations
Chromothripsis
Cirrhosis, Familial
CLAPO Syndrome
Cleidorhizomelic Syndrome
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA
Collagenoma, Familial Cutaneous
COMPLEMENT COMPONENT 2 DEFICIENCY
Complement Component 3 Deficiency, Autosomal Recessive
Complement Component 4, Partial Deficiency Of
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
Composite Lymphoma
Contrecoup Injury
Corneodermatoosseous Syndrome
Coronary Artery Disease
Coronary Artery Disease, Autosomal Dominant 2
Coronary Artery Disease, Autosomal Dominant, 1
Coronary Artery Disease, Development Of, In HIV
Coronary Stenosis
Coxoauricular Syndrome
Cranioacrofacial Syndrome
Craniofaciofrontodigital Syndrome
Craniomicromelic Syndrome
Crome Syndrome
Cryofibrinogenemia, Familial Primary
Cryptotia, Familial
Curatolo Cilio Pessagno Syndrome
CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL
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
Disease Progression
Diseases
Drachtman Weinblatt Sitarz Syndrome
Dystonia
Dystonia With Cerebellar Atrophy
Dystonia With Ringbinden
Dystonia, Dopa-responsive
Erythema
Erythema Elevatum Diutinum
Erythema Palmare Hereditarium
Esophageal Ring, Lower
Esophageal Squamous Cell Carcinoma
Faciocardiomelic Syndrome
Faciocardiorenal Syndrome
Factor 8 Deficiency, Acquired
Failed Back Surgery Syndrome
Fairbank Disease
Familial Dermographism
Familial Hyperbeta- And Prebetalipoproteinemia
Familial Primary Biliary Cirrhosis
Familial Primary Gastric Lymphoma
Familial Streblodactyly
Fanconi Anemia
Fanconi Like Syndrome
Fibrosis
FLOTCH Syndrome
Flynn Aird Syndrome
Fountain 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
Genomic Instability
Giacheti Syndrome
Gigantiform Cementoma, Familial
Glioblastoma
Glioma
Glioma Of Brain, Familial
Glycoprotein IA Deficiency
Gollop Coates Syndrome
GOMBO Syndrome
Granddad Syndrome
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
Hapnes Boman Skeie Syndrome
Hardikar Syndrome
Heart Diseases
Hepatic Adenomas, Familial
Hepatitis
Hepatitis B
Hereditary Breast And Ovarian Cancer Syndrome
Hereditary Koilonychia
Herrmann Syndrome
Hersh Podruch Weisskopk Syndrome
HLA Class 1 Deficiency
Hodgkin Disease
Hooft Disease
Hordnes Engebretsen Knudtson Syndrome
Human Balantidiasis
Hunt's Syndrome
Hyperexplexia Hereditary
Hyperreninemic Hypoaldosteronism, Familial, 2
Hypertrophy
Hypoadrenocorticism, Familial
Hypoglossia, Isolated
Hypoxia
Idiopathic Juxtafoveal Retinal Telangiectasia
Iida Kannari Syndrome
Iliotibial Band Syndrome
Immune Deficiency, Familial Variable
IMMUNODEFICIENCY 11
IMMUNODEFICIENCY 12
IMMUNODEFICIENCY 14
IMMUNODEFICIENCY 15
IMMUNODEFICIENCY 16
IMMUNODEFICIENCY 17
IMMUNODEFICIENCY 18
IMMUNODEFICIENCY 19
IMMUNODEFICIENCY 20
IMMUNODEFICIENCY 21
IMMUNODEFICIENCY 22
IMMUNODEFICIENCY 23
IMMUNODEFICIENCY 24
IMMUNODEFICIENCY 28
IMMUNODEFICIENCY 29
IMMUNODEFICIENCY 30
IMMUNODEFICIENCY 36
IMMUNODEFICIENCY 37
IMMUNODEFICIENCY 39
IMMUNODEFICIENCY 40
IMMUNODEFICIENCY 42
IMMUNODEFICIENCY 44
IMMUNODEFICIENCY 45
IMMUNODEFICIENCY 46
IMMUNODEFICIENCY 47
IMMUNODEFICIENCY 48
IMMUNODEFICIENCY 49
IMMUNODEFICIENCY 50
IMMUNODEFICIENCY 51
Immunodeficiency Syndrome, Variable
Infection
Inflammation
Insulin Receptor, Defect In
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
Lelis Syndrome
Lemierre Syndrome
Leukemia
Leukemia, Acute, X-Linked
Leukoplakia
Lymphoblastic Transformation, Inhibition Of
Lymphoblastic Transformation, Intrinsic Defect In
Lymphoma
Lymphoma, Large B-Cell, Diffuse
Lyngstadaas Syndrome
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
Meningioma
Meningioma, Familial
Meralgia Paraesthetica, Familial
Merlob Grunebaum Reisner Syndrome
Meyenburg-Altherr-Uehlinger Syndrome
Microsatellite Instability
Microtrauma, Physical
Mirizzi Syndrome
MITOCHONDRIAL DNA DEPLETION SYNDROME 11
Mitochondrial Phosphate Carrier Deficiency
Mollica Pavone Antener Syndrome
MOMES Syndrome
Mononen Karnes Senac Syndrome
Morgellons Disease
Multiple Chronic Conditions
Nasodigitoacoustic Syndrome
Nasopharyngeal Carcinoma
Nathalie Syndrome
Neoplasms
Neuroblastoma
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6
Neurodegenerative Diseases
Neuroendocrine Tumors
Neurofaciodigitorenal Syndrome
Nevo Syndrome
Nicolau Syndrome
Nievergelt Syndrome
Nijmegen Breakage Syndrome
Nivelon Nivelon Mabille Syndrome
Oculoauriculofrontonasal Syndrome
Oculocerebrocutaneous Syndrome
Oculodental Syndrome Rutherfurd Syndrome
Oculootoradial Syndrome
Oculopalatocerebral Syndrome
Oculopalatoskeletal Syndrome
Oculorenocerebellar Syndrome
Onat Syndrome
OOCYTE MATURATION DEFECT 1
OOCYTE MATURATION DEFECT 2
Opticocochleodentate Degeneration
Oroticaciduria 1
Oslam Syndrome
Osteosarcoma
Otoonychoperoneal Syndrome
Pachydermodactyly, Familial
Pancreatic Cancer, Adult
Pancreatic Carcinoma, Familial
Pancreatic Lymphoma, Familial
Paraphilic Disorders
Parotidomegaly, Hereditary Bilateral
Pascual Castroviejo Syndrome
Pashayan Syndrome
Passovoy Factor
Pavone Fiumara Rizzo Syndrome
Pechet Factor Deficiency
PHACE Association
Pilotto Syndrome
Piriformis Muscle Syndrome
Piussan Lenaerts Mathieu Syndrome
Pneumonia
Podder-Tolmie Syndrome
Polycystic Ovary Syndrome
Polythelia, Familial
Postthrombotic Syndrome
Preeyasombat Varavithya Syndrome
PREIMPLANTATION EMBRYONIC LETHALITY 1
PREIMPLANTATION EMBRYONIC LETHALITY 2
Primary Dysautonomias
Propping Zerres Syndrome
Prostate Cancer, Familial
PROSTATE CANCER, HEREDITARY, 1
Prostate Cancer, Hereditary, 12
Prostate Cancer, Hereditary, 13
Prostate Cancer, Hereditary, 6
Prostate Cancer, Hereditary, 8
PROSTATE CANCER, HEREDITARY, X-LINKED 1
Pseudoaminopterin Syndrome
Pseudoarylsulfatase A Deficiency
Pseudotrisomy 13 Syndrome
Qazi Markouizos Syndrome
Radiation Induced Meningioma
Radiation Pneumonitis
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant
Rambaud Galian Syndrome
Ramer Ladda Syndrome
Reactive Angioendotheliomatosis
Recurrence
Reginato Schiapachasse Syndrome
Retinoblastoma
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
Schizophrenia
Schlegelberger Grote Syndrome
Schofer Beetz Bohl Syndrome
Scholte Syndrome
Schrander-Stumpel Theunissen Hulsmans Syndrome
Seaver Cassidy Syndrome
Seemanova Lesny Syndrome
Sener Syndrome
Shapiro Syndrome
Shock
Silengo Lerone Pelizza Syndrome
Sillence Syndrome
Sohval Soffer Syndrome
Splenoportal Vascular Anomalies
Starvation
Steinfeld Syndrome
Summitt Syndrome
SUNCT Syndrome
SUPPRESSOR OF TUMORIGENICITY 3
Susac Syndrome
Syndrome
Syringomas, Multiple
T Cell Immunodeficiency Primary
Tabatznik Syndrome
Tatsumi Factor Deficiency
Telangiectasia, Generalized Essential
Three M Syndrome 2
Thyrocerebral-retinal Syndrome
Thyroid Cancer, Papillary
Tonoki Syndrome
Translocation, Genetic
Trichodental Syndrome
Trisomy
Trisomy 13 Syndrome
Trueb Burg Bottani Syndrome
Tsukahara Syndrome
Tucker Syndrome
Upington Disease
Varicella, Severe Recurrent
Velofacioskeletal Syndrome
Verloove-Vanhorick Brubakk Syndrome
Volcke Soekarman Syndrome
Walbaum Titran Durieux Crepin Syndrome
Waldmann Disease
Warburton Anyane Yeboa Syndrome
Warman Mulliken Hayward Syndrome
Waterborne Diseases
Weismann Netter Syndrome
Wyburn Mason's Syndrome
X-Linked Combined Immunodeficiency Diseases
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: ATM FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: ATM-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping