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ARMS2 FISH Probe

The ARMS2 FISH probe is designed to hybridize to the ARMS2 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
ARMS2-20-OR  (Standard Design) 20 (40 μL) 200 μL
ARMS2-20-RE 20 (40 μL) 200 μL
ARMS2-20-GO 20 (40 μL) 200 μL
ARMS2-20-GR 20 (40 μL) 200 μL
ARMS2-20-AQ 20 (40 μL) 200 μL
ARMS2-20-DIG 20 (40 μL) 200 μL
ARMS2-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene encodes a small secreted protein specific to primates. This protein is a component of the choroidal extracellular matrix of the eye. Mutations in this gene are associated with age-related macular degeneration. [provided by RefSeq, Sep 2017]

Gene Details

Gene Symbol: ARMS2

Gene Name: Age-related Maculopathy Susceptibility 2

Chromosome: CHR10: 124214178-124216868

Locus: 10q26.13

Gene Diseases

The ARMS2 gene has been associated with the following diseases:

Disease Name
2-Hydroxyglutaricaciduria
Adactylia, Unilateral
Androblastoma Of Ovary
Angiolipomatosis, Familial
Atrophy
Bankart Lesions
Blount Disease
Brachymesophalangy 2 And 5
Campomelia Cumming Type
Central Serous Chorioretinopathy
Choroidal Neovascularization
COMPLEMENT COMPONENT 2 DEFICIENCY
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I
Coronary Artery Disease
Coronary Artery Disease, Autosomal Dominant 2
Coronary Artery Disease, Autosomal Dominant, 1
Cryofibrinogenemia, Familial Primary
Cryptotia, Familial
Dermatoosteolysis Kirghizian Type
Dieterich's Disease
Dimauro Disease
Disease
Drusen, Radial, Autosomal Dominant
Fairbank Disease
Familial Dermographism
Familial Hyperbeta- And Prebetalipoproteinemia
Familial Streblodactyly
Freiberg's Disease
Geographic Atrophy
Gigantiform Cementoma, Familial
Grover's Disease
Histoplasmosis
Hooft Disease
Human Balantidiasis
Hyperreninemic Hypoaldosteronism, Familial, 2
Hypertension
Hypoadrenocorticism, Familial
Infection
Kuskokwim Disease
Kyrle Disease
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
Marchiafava-Bignami Disease
Meralgia Paraesthetica, Familial
Morgellons Disease
Myopia
Myopia 11
MYOPIA 21, AUTOSOMAL DOMINANT
MYOPIA 22, AUTOSOMAL DOMINANT
MYOPIA 24, AUTOSOMAL DOMINANT
MYOPIA 25, AUTOSOMAL DOMINANT
Opticocochleodentate Degeneration
Oroticaciduria 1
Pachydermodactyly, Familial
Paraphilic Disorders
Passovoy Factor
Pechet Factor Deficiency
PHACE Association
Pneumonia
Polythelia, Familial
Primary Dysautonomias
Protein Deficiency
Pseudoarylsulfatase A Deficiency
Recurrence
Renoprival Hypertension
Ribbing Disease
Sakoda Complex
Tatsumi Factor Deficiency
Upington Disease
Waldmann Disease
Wet Macular Degeneration
Yusho Disease
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: ARMS2 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: ARMS2-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping