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ACTA1 FISH Probe

The ACTA1 FISH probe is designed to hybridize to the ACTA1 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
ACTA1-20-OR  (Standard Design) 20 (40 μL) 200 μL
ACTA1-20-RE 20 (40 μL) 200 μL
ACTA1-20-GO 20 (40 μL) 200 μL
ACTA1-20-GR 20 (40 μL) 200 μL
ACTA1-20-AQ 20 (40 μL) 200 μL
ACTA1-20-DIG 20 (40 μL) 200 μL
ACTA1-20-BIO 20 (40 μL) 200 μL

Gene Summary

The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol: ACTA1

Gene Name: Actin, Alpha 1, Skeletal Muscle

Chromosome: CHR1: 229566992-229569843

Locus: 1q42.13

Gene Diseases

The ACTA1 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
Acrootoocular Syndrome
Acrorenal Syndrome
Acrorenal Syndrome Recessive
Akaba Hayasaka Syndrome
Akesson Syndrome
Aloi Tomasini Isaia Syndrome
Alsing Syndrome
Ameloonychohypohidrotic Syndrome
Ansell Bywaters Elderking Syndrome
Arakawa Syndrome 2
AREDYLD Syndrome
Arima Syndrome
Athrombia, Essential
Aughton Syndrome
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3
Ayazi Syndrome
BADS Syndrome
Baetz-Greenwalt Syndrome
Bagatelle Cassidy Syndrome
Bangstad Syndrome
Banki Syndrome
Banti's Syndrome
Basaran Yilmaz Syndrome
Bassoe Syndrome
Bazopoulou Kyrkanidou Syndrome
Beardwell Syndrome
Beemer Ertbruggen Syndrome
Bellini Chiumello Rimoldi Syndrome
Blepharo-cheilo-dontic Syndrome
Blount Disease
Boerhaave Syndrome
Bonneau Syndrome
Boudhina Yedes Khiari Syndrome
Brachioskeletogenital Syndrome
Brachymesophalangy 2 And 5
Brunoni Syndrome
CAHMR Syndrome
Calabro Syndrome
CAMFAK Syndrome
Campomelia Cumming Type
Cancer
CANOMAD Syndrome
Cantalamessa Baldini Ambrosi Syndrome
Carcinogenesis
Cardiocranial Syndrome
Cardiomyopathy
Carrington Syndrome
CATSHL Syndrome
Cerebrooculonasal Syndrome
Chilaiditi Syndrome
Childhood Myocerebrohepatopathy Spectrum
Chromosome 1 Ring
CLAPO Syndrome
Cleidorhizomelic Syndrome
Contrecoup Injury
Corneodermatoosseous Syndrome
Coxoauricular Syndrome
Cranioacrofacial Syndrome
Craniofaciofrontodigital Syndrome
Craniomicromelic Syndrome
Crome Syndrome
Curatolo Cilio Pessagno Syndrome
D-glycericacidemia
Daentl Towsend Siegel Syndrome
Daish Hardman Lamont Syndrome
Daneman Davy Mancer Syndrome
Davenport Donlan Syndrome
Death
Dengue
Dermatoosteolysis Kirghizian Type
Devriendt Syndrome
Dieterich's Disease
Digitorenocerebral Syndrome
Dimauro Disease
Disease
Diseases
Drachtman Weinblatt Sitarz Syndrome
Faciocardiomelic Syndrome
Faciocardiorenal Syndrome
Fairbank Disease
Fascial Dystrophy, Congenital
Fetal Trimethadione Syndrome
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
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
Herrmann Syndrome
Hersh Podruch Weisskopk Syndrome
Hooft Disease
Hordnes Engebretsen Knudtson Syndrome
Human Balantidiasis
Hunt's Syndrome
Hypertaurinuric Cardiomyopathy
Iida Kannari Syndrome
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
Infantile Polymyoclonus
Infection
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
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
Muscle Weakness
Muscular Dystrophy, Cardiac Type
Muscular Dystrophy, Progressive Pectorodorsal
Myofibrillar Myopathy
Myositis
Myotonic Dystrophy
Nasodigitoacoustic Syndrome
Nathalie Syndrome
Neurofaciodigitorenal Syndrome
Nevo Syndrome
Nicolau Syndrome
Nievergelt Syndrome
Nivelon Nivelon Mabille Syndrome
Oculoauriculofrontonasal Syndrome
Oculocerebrocutaneous Syndrome
Oculodental Syndrome Rutherfurd Syndrome
Oculootoradial Syndrome
Oculopalatocerebral Syndrome
Oculopalatoskeletal Syndrome
Oculopharyngodistal Myopathy
Oculorenocerebellar Syndrome
Onat Syndrome
Ophthalmoplegia
Oroticaciduria 1
Oslam Syndrome
Otoonychoperoneal Syndrome
Ovarian Epithelial Cancer
Pascual Castroviejo Syndrome
Pashayan Syndrome
Passovoy Factor
Pavone Fiumara Rizzo Syndrome
PHACE Association
Pilotto Syndrome
Piriformis Muscle Syndrome
Piussan Lenaerts Mathieu Syndrome
Podder-Tolmie Syndrome
Postthrombotic Syndrome
Preeyasombat Varavithya Syndrome
Primary Dysautonomias
Propping Zerres Syndrome
Protein Aggregation, Pathological
Pseudoaminopterin Syndrome
Pseudotrisomy 13 Syndrome
Qazi Markouizos Syndrome
Rambaud Galian Syndrome
Ramer Ladda Syndrome
Recurrence
Reginato Schiapachasse Syndrome
Retinohepatoendocrinologic Syndrome
RHYNS Syndrome
Ribbing Disease
Richards-Rundle Syndrome
Rombo Syndrome
Rosselli-Gulienetti Syndrome
Rudiger Syndrome
Sakoda Complex
Salcedo Syndrome
Sammartino De Crecchio Syndrome
Sandifer Syndrome
Satoyoshi Syndrome
Schlegelberger Grote Syndrome
Schofer Beetz Bohl Syndrome
Scholte Syndrome
Schrander-Stumpel Theunissen Hulsmans Syndrome
Scoliosis
Seaver Cassidy Syndrome
Seemanova Lesny Syndrome
Sener Syndrome
Sepsis
Shapiro Syndrome
Silengo Lerone Pelizza Syndrome
Sillence Syndrome
Sohval Soffer Syndrome
Splenogonadal Fusion Limb Defects Micrognatia
Steinfeld Syndrome
Sulfhemoglobinemia, Congenital
Summitt Syndrome
SUNCT Syndrome
Susac Syndrome
Syndrome
Syringomas, Multiple
T Cell Immunodeficiency Primary
Tabatznik Syndrome
Tonoki Syndrome
Trichodental Syndrome
Trueb Burg Bottani Syndrome
Tsukahara Syndrome
Tucker Syndrome
Upington Disease
Vaccinia
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
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: ACTA1 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: ACTA1-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping