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ABCB6 FISH Probe

The ABCB6 FISH probe is designed to hybridize to the ABCB6 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
ABCB6-20-OR  (Standard Design) 20 (40 μL) 200 μL
ABCB6-20-RE 20 (40 μL) 200 μL
ABCB6-20-GO 20 (40 μL) 200 μL
ABCB6-20-GR 20 (40 μL) 200 μL
ABCB6-20-AQ 20 (40 μL) 200 μL
ABCB6-20-DIG 20 (40 μL) 200 μL
ABCB6-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ABC proteins transport various molecules across extra- and intra-cellular membranes. This protein is a member of the heavy metal importer subfamily and plays a role in porphyrin transport. This gene is the molecular basis of the Langereis (Lan) blood group antigen and mutations in this gene underlie familial pseudohyperkalemia and dyschromatosis universalis hereditaria. [provided by RefSeq, Mar 2017]

Gene Details

Gene Symbol: ABCB6

Gene Name: ATP Binding Cassette Subfamily B Member 6 (Langereis Blood Group)

Chromosome: CHR2: 220074487-220083712

Locus: 2q35

Gene Diseases

The ABCB6 gene has been associated with the following diseases:

Disease Name
2-Hydroxyglutaricaciduria
Abc Disease
Androblastoma Of Ovary
Angiolipomatosis, Familial
Blount Disease
Bone Anteversion
Bone Retroversion
Brachymesophalangy 2 And 5
Campomelia Cumming Type
Carcinoma
Coloboma
Cryofibrinogenemia, Familial Primary
Cryptotia, Familial
Dermatoosteolysis Kirghizian Type
Dieterich's Disease
Dimauro Disease
Disease
Dyschromatosis Universalis Hereditaria
Dyschromatosis Universalis Hereditaria 1
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
Fairbank Disease
Familial Dermographism
Familial Hyperbeta- And Prebetalipoproteinemia
Familial Streblodactyly
Freiberg's Disease
Gigantiform Cementoma, Familial
Glioma
Glioma Of Brain, Familial
Grover's Disease
Hooft Disease
Human Balantidiasis
Hyperreninemic Hypoaldosteronism, Familial, 2
Hypoadrenocorticism, Familial
Hypoglossia, Isolated
Kuskokwim Disease
Kyrle Disease
Leukemia
Marchiafava-Bignami Disease
Meralgia Paraesthetica, Familial
Microphthalmia, Isolated 1
Microphthalmia, Isolated 2
Microphthalmia, Isolated 3
Microphthalmia, Isolated 4
MICROPHTHALMIA, ISOLATED 5
MICROPHTHALMIA, ISOLATED 7
MICROPHTHALMIA, ISOLATED 8
Microphthalmia, Isolated, With Coloboma 1
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10
Microphthalmia, Isolated, With Coloboma 2
Microphthalmia, Isolated, With Coloboma 3
Microphthalmia, Isolated, With Coloboma 4
Microphthalmia, Isolated, With Coloboma 5
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9
Microphthalmia, Isolated, With Corectopia
Morgellons Disease
Oroticaciduria 1
Pachydermodactyly, Familial
Passovoy Factor
PHACE Association
Polythelia, Familial
Primary Dysautonomias
Recurrence
Ribbing Disease
Sakoda Complex
Upington Disease
Waldmann Disease
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: ABCB6 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: ABCB6-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping