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AICDA FISH Probe

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

Gene Summary

This gene encodes a RNA-editing deaminase that is a member of the cytidine deaminase family. The protein is involved in somatic hypermutation, gene conversion, and class-switch recombination of immunoglobulin genes. Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by RefSeq, Feb 2009]

Gene Details

Gene Symbol: AICDA

Gene Name: Activation Induced Cytidine Deaminase

Chromosome: CHR12: 8754761-8765442

Locus: 12p13.31

Gene Diseases

The AICDA 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
Acquired Hypoprothrombinemia
Acrocephalopolydactylous Dysplasia
Acrootoocular Syndrome
Acrorenal Syndrome
Acrorenal Syndrome Recessive
Adenocarcinoid Tumor
Adenocarcinoma
Akaba Hayasaka Syndrome
Akesson Syndrome
Aloi Tomasini Isaia Syndrome
Alsing Syndrome
Ameloonychohypohidrotic Syndrome
Ansell Bywaters Elderking Syndrome
Arakawa Syndrome 2
AREDYLD Syndrome
Arima Syndrome
Arthritis
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
Blast Crisis
Blepharo-cheilo-dontic Syndrome
Blount Disease
Boerhaave Syndrome
Bone Anteversion
Bone Retroversion
Bonneau Syndrome
Boudhina Yedes Khiari Syndrome
Brachioskeletogenital Syndrome
Brachycephalofrontonasal Dysplasia
Brachymesophalangy 2 And 5
Brunoni Syndrome
Burkitt Lymphoma
CAHMR Syndrome
Calabro Syndrome
CAMFAK Syndrome
Campomelia Cumming Type
Cancer
CANOMAD Syndrome
Cantalamessa Baldini Ambrosi Syndrome
Carcinogenesis
Carcinoma
Cardiocranial Syndrome
Carrington Syndrome
CATSHL Syndrome
Cerebrooculonasal Syndrome
Chilaiditi Syndrome
Cholangiocarcinoma
Chromosome 12 Ring
CLAPO Syndrome
Cleidorhizomelic Syndrome
Colitis
Colitis, Lymphocytic
Common Variable Immunodeficiency
Corneodermatoosseous Syndrome
Coxoauricular Syndrome
Cranioacrofacial Syndrome
Craniofaciofrontodigital Syndrome
Craniomicromelic Syndrome
Craniotelencephalic Dysplasia
Crome Syndrome
Curatolo Cilio Pessagno Syndrome
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
Diseases
Drachtman Weinblatt Sitarz Syndrome
Dysplasia Epiphysealis Hemimelica
Faciocardiomelic Syndrome
Faciocardiorenal Syndrome
Factor 8 Deficiency, Acquired
Fairbank Disease
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
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
Hepatitis
Hepatitis B
Herrmann Syndrome
Hersh Podruch Weisskopk Syndrome
Hooft Disease
Hordnes Engebretsen Knudtson Syndrome
Human Balantidiasis
Hunt's Syndrome
Hyper-Beta-Alaninemia
Hyper-IgM Immunodeficiency Syndrome, Type 1
IgA Deficiency
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
IMMUNODEFICIENCY 51
Immunodeficiency Syndrome, Variable
Immunodeficiency With Hyper-Igm, Type 4
Immunoglobulin A Deficiency 1
Immunoglobulin A Deficiency 2
Infection
Inflammation
Influenza, Human
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
Kyphomelic Dysplasia
Kyrle Disease
Lachiewicz Sibley Syndrome
Lacrimoauriculodentodigital Syndrome
Lambotte Syndrome
Lelis Syndrome
Lemierre Syndrome
Leukemia
Lymphoblastic Transformation, Inhibition Of
Lymphoma
Lymphoma, Large B-Cell, Diffuse
Lyngstadaas Syndrome
Malaria
Malignant Mesenchymal Tumor
Malignant Teratocarcinosarcoma
Malouf Syndrome
Manouvrier Syndrome
Marchiafava-Bignami Disease
Marsden Syndrome
Massa Casaer Ceulemans Syndrome
May-Thurner Syndrome
Mehes Syndrome
Melanoma
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
Multiple Chronic Conditions
Nasodigitoacoustic Syndrome
Nathalie Syndrome
Neoplasms
Neurofaciodigitorenal Syndrome
Nevo Syndrome
Nicolau Syndrome
Nievergelt Syndrome
Nivelon Nivelon Mabille Syndrome
Oculoauriculofrontonasal Syndrome
Oculocerebrocutaneous Syndrome
Oculodental Syndrome Rutherfurd Syndrome
Oculodentoosseous Dysplasia Recessive
Oculootofacial Dysplasia
Oculootoradial Syndrome
Oculopalatocerebral Syndrome
Oculopalatoskeletal Syndrome
Oculorenocerebellar Syndrome
Odontomicronychial Dysplasia
Onat Syndrome
Ophthalmomandibulomelic Dysplasia
Oroticaciduria 1
Oslam Syndrome
Otoonychoperoneal Syndrome
Pascual Castroviejo Syndrome
Pashayan Syndrome
Passovoy Factor
Pavone Fiumara Rizzo Syndrome
Pechet Factor Deficiency
Pelviscapular Dysplasia
PHACE Association
Philadelphia Chromosome
Pilotto Syndrome
Piussan Lenaerts Mathieu Syndrome
Podder-Tolmie Syndrome
Postthrombotic Syndrome
Preeyasombat Varavithya Syndrome
Primary Dysautonomias
Propping Zerres Syndrome
Pseudoaminopterin Syndrome
Pseudoarylsulfatase A Deficiency
Pseudodiastrophic Dysplasia
Pseudotrisomy 13 Syndrome
Qazi Markouizos Syndrome
Rambaud Galian Syndrome
Ramer Ladda Syndrome
Reginato Schiapachasse Syndrome
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
Sjogren's Syndrome
Sohval Soffer Syndrome
Steinfeld Syndrome
Summitt Syndrome
SUNCT Syndrome
Susac Syndrome
Syndrome
Syringomas, Multiple
T Cell Immunodeficiency Primary
Tabatznik Syndrome
Tatsumi Factor Deficiency
Thoracolaryngopelvic Dysplasia
Thoracomelic Dysplasia
Tonoki Syndrome
Translocation, Genetic
Trichodental Syndrome
Trichoodontoonychial Dysplasia
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: AICDA FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: AICDA-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping