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Gene-specific Break Apart Probe-XBP1

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Catalog: GBAFP-XBP1-09159
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (XBP1). 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: XBP1 Gene-specific Break Apart Probe is designed to detect potential XBP1 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 X-box Binding Protein 1
Gene Summary [Provided by RefSeq] This gene encodes a transcription factor that regulates MHC class II genes by binding to a promoter element referred to as an X box. This gene product is a bZIP protein, which was also identified as a cellular transcription factor that binds to an enhancer in the promoter of the T cell leukemia virus type 1 promoter. It may increase expression of viral proteins by acting as the DNA binding partner of a viral transactivator. It has been found that upon accumulation of unfolded proteins in the endoplasmic reticulum (ER), the mRNA of this gene is processed to an active form by an unconventional splicing mechanism that is mediated by the endonuclease inositol-requiring enzyme 1 (IRE1). The resulting loss of 26 nt from the spliced mRNA causes a frame-shift and an isoform XBP1(S), which is the functionally active transcription factor. The isoform encoded by the unspliced mRNA, XBP1(U), is constitutively expressed, and thought to function as a negative feedback regulator of XBP1(S), which shuts off transcription of target genes during the recovery phase of ER stress. A pseudogene of XBP1 has been identified and localized to chromosome 5. [provided by RefSeq, Jul 2008]
Gene Symbol XBP1
Location 22q12
Chromosome Chromosome22
Coordinates This gene maps to 29190547-29196560 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 GR; OR GBAFP-XBP1-09159-GROR 515nm;573nm 491nm;548nm
2 AQ; OR GBAFP-XBP1-09159-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-XBP1-09159-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-XBP1-09159-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-XBP1-09159-GRGO 515nm;551nm 491nm;525nm
6 GR; RE GBAFP-XBP1-09159-GRRE 515nm;599nm 491nm;580nm
7 OR; GR GBAFP-XBP1-09159-ORGR 573nm;515nm 548nm;491nm
8 RE; GO GBAFP-XBP1-09159-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-XBP1-09159-REGR 599nm;515nm 580nm;491nm

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