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Gene-specific Break Apart Probe-B4GALT7

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Catalog: GBAFP-B4GALT7-10117
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (B4GALT7). 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: B4GALT7 Gene-specific Break Apart Probe is designed to detect potential B4GALT7 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 Beta-1,4-galactosyltransferase 7
Gene Summary [Provided by RefSeq] This gene is a member of the beta-1,4-galactosyltransferase (beta4GalT) family. Family members encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose. Each beta4GalT member has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures. As type II membrane proteins, they have an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus which then remains uncleaved to function as a transmembrane anchor. The enzyme encoded by this gene attaches the first galactose in the common carbohydrate-protein linkage (GlcA-beta1,3-Gal-beta1,3-Gal-beta1,4-Xyl-beta1-O-Ser) found in proteoglycans. This enzyme differs from other beta4GalTs because it lacks the conserved Cys residues found in beta4GalT1-beta4GalT6 and it is located in cis-Golgi instead of trans-Golgi. Mutations in this gene have been associated with the progeroid form of Ehlers-Danlos syndrome. [provided by RefSeq, Oct 2009]
Gene Symbol B4GALT7
Location 5q35.3
Chromosome Chromosome5
Coordinates This gene maps to 177027118-177037346 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR; GR GBAFP-B4GALT7-10117-ORGR 573nm;515nm 548nm;491nm
2 AQ; OR GBAFP-B4GALT7-10117-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-B4GALT7-10117-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-B4GALT7-10117-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-B4GALT7-10117-GRGO 515nm;551nm 491nm;525nm
6 GR; OR GBAFP-B4GALT7-10117-GROR 515nm;573nm 491nm;548nm
7 GR; RE GBAFP-B4GALT7-10117-GRRE 515nm;599nm 491nm;580nm
8 RE; GO GBAFP-B4GALT7-10117-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-B4GALT7-10117-REGR 599nm;515nm 580nm;491nm

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