Gene-specific Copy Number Variation Probe-RPL36A-HNRNPH2

Add to Cart

Catalog:	CNVFP-RPL36A-HNRNPH2-17555
Classification:	Copy Number Variation
Description:	Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RPL36A-HNRNPH2). 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:	RPL36A-HNRNPH2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RPL36A-HNRNPH2 genes. This product achieves the purpose of detection by hybridizing with the RPL36A-HNRNPH2 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH.
Quantity:	20 Tests
Probe Kits Volume (µL):	40 μL
Hybridization Solution (µL):	200 μL
Turnaround Time:	7-10 Business Days
Shipping Time:	1-2 Day Expedited Shipping
Shipping Conditions:	-20℃
Storage Conditions:	Store at -20℃ and avoid light;

Gene Name	RPL36A-HNRNPH2 Readthrough
Gene Summary [Provided by RefSeq]	This locus represents naturally occurring read-through transcription between the neighboring ribosomal protein L36a and heterogeneous nuclear ribonucleoprotein H2 (H') genes on chromosome X. The read-through transcript produces a protein with similarity to the protein encoded by the upstream locus, ribosomal protein L36a. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jan 2011]
Gene Symbol	RPL36A-HNRNPH2
Location	Xq22.1
Chromosome	ChromosomeX
Coordinates	This gene maps to 100645877-100669128 in GRCh37 coordinates.
Species	Human

Other Products

CONTACT SUPPORT

Online Inquiry