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Gene-specific Break Apart Probe-PEX3

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Catalog: GBAFP-PEX3-15767
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PEX3). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent.
Application: PEX3 Gene-specific Break Apart Probe is designed to detect potential PEX3 rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services.
Quantity: 20 Tests
Probe Kits Volume (µL): 40 μL
Hybridization Solution (µL): 200 μL
Turnaround Time: Within 10 Business Days
Shipping Time: 1-2 Day Expedited Shipping
Shipping Conditions: -20℃
Storage Conditions: Store at -20℃ and avoid light;

Gene Details

Gene Name Peroxisomal Biogenesis Factor 3
Gene Summary [Provided by RefSeq] The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
Gene Symbol PEX3
Location 6q24.2
Chromosome Chromosome6
Coordinates This gene maps to 143771917-143811751 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR; GR GBAFP-PEX3-15767-ORGR 573nm;515nm 548nm;491nm
2 AQ; OR GBAFP-PEX3-15767-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-PEX3-15767-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-PEX3-15767-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-PEX3-15767-GRGO 515nm;551nm 491nm;525nm
6 GR; OR GBAFP-PEX3-15767-GROR 515nm;573nm 491nm;548nm
7 GR; RE GBAFP-PEX3-15767-GRRE 515nm;599nm 491nm;580nm
8 RE; GO GBAFP-PEX3-15767-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-PEX3-15767-REGR 599nm;515nm 580nm;491nm

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