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Gene-specific Break Apart Probe-TNFRSF13C

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Catalog: GBAFP-TNFRSF13C-08528
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TNFRSF13C). 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: TNFRSF13C Gene-specific Break Apart Probe is designed to detect potential TNFRSF13C 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 TNF Receptor Superfamily Member 13C
Gene Summary [Provided by RefSeq] B cell-activating factor (BAFF) enhances B-cell survival in vitro and is a regulator of the peripheral B-cell population. Overexpression of Baff in mice results in mature B-cell hyperplasia and symptoms of systemic lupus erythematosus (SLE). Also, some SLE patients have increased levels of BAFF in serum. Therefore, it has been proposed that abnormally high levels of BAFF may contribute to the pathogenesis of autoimmune diseases by enhancing the survival of autoreactive B cells. The protein encoded by this gene is a receptor for BAFF and is a type III transmembrane protein containing a single extracellular cysteine-rich domain. It is thought that this receptor is the principal receptor required for BAFF-mediated mature B-cell survival. [provided by RefSeq, Jul 2008]
Gene Symbol TNFRSF13C
Location 22q13.2
Chromosome Chromosome22
Coordinates This gene maps to 42321035-42322821 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 GR; OR GBAFP-TNFRSF13C-08528-GROR 515nm;573nm 491nm;548nm
2 AQ; OR GBAFP-TNFRSF13C-08528-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-TNFRSF13C-08528-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-TNFRSF13C-08528-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-TNFRSF13C-08528-GRGO 515nm;551nm 491nm;525nm
6 GR; RE GBAFP-TNFRSF13C-08528-GRRE 515nm;599nm 491nm;580nm
7 OR; GR GBAFP-TNFRSF13C-08528-ORGR 573nm;515nm 548nm;491nm
8 RE; GO GBAFP-TNFRSF13C-08528-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-TNFRSF13C-08528-REGR 599nm;515nm 580nm;491nm

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