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ABCA3 Break Apart FISH Probe

Empire Genomics’ ABCA3 Break Apart FISH Probe is designed to flank the ABCA3 gene and is typically used for detecting ABCA3 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping

Download FISH ProtocolDownload Material Safety Data Sheet

SKU Test Kits Buffer Dye Color Order Now
ABCA3BA-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
ABCA3BA-20-GORE 20 (40 μL) 200 μL
ABCA3BA-20-REGO 20 (40 μL) 200 μL
ABCA3BA-20-REGR 20 (40 μL) 200 μL
ABCA3BA-20-GOGR 20 (40 μL) 200 μL
ABCA3BA-20-GRRE 20 (40 μL) 200 μL
ABCA3BA-20-GROR 20 (40 μL) 200 μL
ABCA3BA-20-GRGO 20 (40 μL) 200 μL
ABCA3BA-20-AQOR 20 (40 μL) 200 μL

Gene Summary

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. The full transporter encoded by this gene may be involved in development of resistance to xenobiotics and engulfment during programmed cell death. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol: ABCA3

Gene Name: ATP Binding Cassette Subfamily A Member 3

Chromosome: CHR16: 2325878-2390747

Locus: 16p13.3

Gene Diseases

The following diseases have been found to be related to the ABCA3 gene.

2-Hydroxyglutaricaciduria
49,XXXXX Syndrome
Aagenaes Syndrome
Abc Disease
Abderhalden-Kaufmann-Lignac Syndrome
Achard Syndrome
Achard-Thiers Syndrome
Acrocephalopolysyndactyly Type II
Acrootoocular Syndrome
Acrorenal Syndrome
Adrenal Insufficiency, Congenital
Akaba Hayasaka Syndrome
Akesson Syndrome
Aloi Tomasini Isaia Syndrome
Alsing Syndrome
Ameloonychohypohidrotic Syndrome
Angiolipomatosis, Familial
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
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
Boerhaave Syndrome
Bonneau Syndrome
Boudhina Yedes Khiari Syndrome
Brachioskeletogenital Syndrome
Brachymesophalangy 2 And 5
Breast Cancer, Familial
Broad-Betalipoproteinemia
Brunoni Syndrome
CAHMR Syndrome
Calabro Syndrome
CAMFAK Syndrome
Campomelia Cumming Type
Cancer
CANOMAD Syndrome
Cantalamessa Baldini Ambrosi Syndrome
Cardiocranial Syndrome
Carrington Syndrome
Cataract
CATARACT 36
CATARACT 41
CATARACT 42
CATARACT 43
CATARACT 45
Cataract Microcornea Syndrome
Cataract, Autosomal Dominant
Cataract, Lamellar 2
CATSHL Syndrome
Cerebrooculonasal Syndrome
Chilaiditi Syndrome
Childhood Myocerebrohepatopathy Spectrum
CLAPO Syndrome
Cleidorhizomelic Syndrome
Corneodermatoosseous Syndrome
Coxoauricular Syndrome
Cranioacrofacial Syndrome
Craniofaciofrontodigital Syndrome
Craniomicromelic Syndrome
Crome Syndrome
Cryofibrinogenemia, Familial Primary
Cryptotia, Familial
Curatolo Cilio Pessagno Syndrome
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
Diseases
Drachtman Weinblatt Sitarz Syndrome
Faciocardiomelic Syndrome
Faciocardiorenal Syndrome
Fairbank Disease
Familial Dermographism
Familial Glucocorticoid Deficiency 1
Familial Hyperbeta- And Prebetalipoproteinemia
Familial Streblodactyly
Fibrosis
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
Gigantiform Cementoma, Familial
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
Herrmann Syndrome
Hersh Podruch Weisskopk Syndrome
Hooft Disease
Hordnes Engebretsen Knudtson Syndrome
Human Balantidiasis
Hunt's Syndrome
Hyperreninemic Hypoaldosteronism, Familial, 2
Hypoadrenocorticism, Familial
Iida Kannari Syndrome
Inflammation
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
Lung Diseases
Lymphoma
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
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
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
Oculorenocerebellar Syndrome
Onat Syndrome
Oroticaciduria 1
Oslam Syndrome
Otoonychoperoneal Syndrome
Pachydermodactyly, Familial
Pascual Castroviejo Syndrome
Pashayan Syndrome
Passovoy Factor
Pavone Fiumara Rizzo Syndrome
Pechet Factor Deficiency
PHACE Association
Pilotto Syndrome
Piussan Lenaerts Mathieu Syndrome
Podder-Tolmie Syndrome
Polythelia, Familial
Postthrombotic Syndrome
Preeyasombat Varavithya Syndrome
Primary Dysautonomias
Propping Zerres Syndrome
Pseudoaminopterin Syndrome
Pseudoarylsulfatase A Deficiency
Pseudotrisomy 13 Syndrome
Pulmonary Fibrosis
Qazi Markouizos Syndrome
Rambaud Galian Syndrome
Ramer Ladda Syndrome
Reginato Schiapachasse Syndrome
Respiratory Distress Syndrome, Newborn
Respiratory Insufficiency
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
Sulfhemoglobinemia, Congenital
Summitt Syndrome
SUNCT Syndrome
Surfactant Metabolism Dysfunction, Pulmonary, 1
Surfactant Metabolism Dysfunction, Pulmonary, 2
Surfactant Metabolism Dysfunction, Pulmonary, 3
Surfactant Metabolism Dysfunction, Pulmonary, 4
Susac Syndrome
Syndrome
Tabatznik Syndrome
Tatsumi Factor Deficiency
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
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: ABCA3 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: ABCA3-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping