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Gene-specific Copy Number Variation Probe-CHGB

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Catalog: CNVFP-CHGB-02609
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CHGB). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services.
Application: CHGB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CHGB genes. This product achieves the purpose of detection by hybridizing with the CHGB gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH.
Category: Copy Number Variation
Probe Kits Volume (µL): 40 μL
Quantity: 20 Tests
Hybridization Solution (µL): 200 μL
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping
Storage Conditions: Store at -20℃ and avoid light;
Shipping Conditions: -20℃

Gene Details

Gene Name Chromogranin B
Gene Summary [Provided by RefSeq] This gene encodes a tyrosine-sulfated secretory protein abundant in peptidergic endocrine cells and neurons. This protein may serve as a precursor for regulatory peptides. [provided by RefSeq, Jan 2009]
Gene Symbol CHGB
Location 20p12.3
Chromosome Chromosome20
Coordinates This gene maps to 5891973-5906005 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-CHGB-02609-OR 573nm 548nm
2 RE CNVFP-CHGB-02609-RE 599nm 580nm
3 GO CNVFP-CHGB-02609-GO 551nm 525nm
4 GR CNVFP-CHGB-02609-GR 515nm 491nm
5 AQ CNVFP-CHGB-02609-AQ 467nm 418nm

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