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Gene-specific Break Apart Probe-PCSK7

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Catalog: GBAFP-PCSK7-06037
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PCSK7). 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: PCSK7 Gene-specific Break Apart Probe is designed to detect potential PCSK7 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 Proprotein Convertase Subtilisin/kexin Type 7
Gene Summary [Provided by RefSeq] This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. It encodes a type 1 membrane bound protease that is expressed in many tissues, including neuroendocrine, liver, gut, and brain. The encoded protein undergoes an initial autocatalytic processing event in the ER and then sorts to the trans-Golgi network through endosomes where a second autocatalytic event takes place and the catalytic activity is acquired. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It can process proalbumin and is thought to be responsible for the activation of HIV envelope glycoproteins gp160 and gp140. This gene has been implicated in the transcriptional regulation of housekeeping genes and plays a role in the regulation of iron metabolism. A t(11;14)(q23;q32) chromosome translocation associated with B-cell lymphoma occurs between this gene and its inverted counterpart. [provided by RefSeq, Feb 2014]
Gene Symbol PCSK7
Location 11q23.3
Chromosome Chromosome11
Coordinates This gene maps to 117075787-117102811 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 GR; OR GBAFP-PCSK7-06037-GROR 515nm;573nm 491nm;548nm
2 AQ; OR GBAFP-PCSK7-06037-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-PCSK7-06037-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-PCSK7-06037-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-PCSK7-06037-GRGO 515nm;551nm 491nm;525nm
6 GR; RE GBAFP-PCSK7-06037-GRRE 515nm;599nm 491nm;580nm
7 OR; GR GBAFP-PCSK7-06037-ORGR 573nm;515nm 548nm;491nm
8 RE; GO GBAFP-PCSK7-06037-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-PCSK7-06037-REGR 599nm;515nm 580nm;491nm

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