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Gene-specific Copy Number Variation Probe-SIGLEC8

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Catalog: CNVFP-SIGLEC8-18337
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SIGLEC8). 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: SIGLEC8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SIGLEC8 genes. This product achieves the purpose of detection by hybridizing with the SIGLEC8 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 Sialic Acid Binding Ig Like Lectin 8
Gene Summary [Provided by RefSeq] Sialic acid-binding immunoglobulin (Ig)-like lectins, or SIGLECs (e.g., CD33 (MIM 159590)), are a family of type 1 transmembrane proteins each having a unique expression pattern, mostly in hemopoietic cells. SIGLEC8 is a member of the CD33-like subgroup of SIGLECs, which are localized to 19q13.3-q13.4 and have 2 conserved cytoplasmic tyrosine-based motifs: an immunoreceptor tyrosine-based inhibitory motif, or ITIM (see MIM 604964), and a motif homologous to one identified in signaling lymphocyte activation molecule (SLAM; MIM 603492) that mediates an association with SLAM-associated protein (SAP; MIM 300490) (summarized by Foussias et al., 2000 [PubMed 11095983]).[supplied by OMIM, May 2010]
Gene Symbol SIGLEC8
Location 19q13.41
Chromosome Chromosome19
Coordinates This gene maps to 51954250-51961708 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-SIGLEC8-18337-OR 573nm 548nm
2 RE CNVFP-SIGLEC8-18337-RE 599nm 580nm
3 GO CNVFP-SIGLEC8-18337-GO 551nm 525nm
4 GR CNVFP-SIGLEC8-18337-GR 515nm 491nm
5 AQ CNVFP-SIGLEC8-18337-AQ 467nm 418nm

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