| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ANXA6-UTRN-20-RERE | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-REOR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-REGO | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-REGR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-REAQ | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-ORRE | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-OROR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-ORGO | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-ORGR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-ORAQ | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GORE | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GOOR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GOGO | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GOGR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GOAQ | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GRRE | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GROR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GRGO | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GRGR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-GRAQ | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-AQRE | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-AQOR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-AQGO | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-AQGR | 20 (40 μL) | 200 μL |
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| ANXA6-UTRN-20-AQAQ | 20 (40 μL) | 200 μL |
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Annexin VI belongs to a family of calcium-dependent membrane and phospholipid binding proteins. Several members of the annexin family have been implicated in membrane-related events along exocytotic and endocytotic pathways. The annexin VI gene is approximately 60 kbp long and contains 26 exons. It encodes a protein of about 68 kDa that consists of eight 68-amino acid repeats separated by linking sequences of variable lengths. It is highly similar to human annexins I and II sequences, each of which contain four such repeats. Annexin VI has been implicated in mediating the endosome aggregation and vesicle fusion in secreting epithelia during exocytosis. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2010]
Gene Symbol : ANXA6
Gene Name : Annexin A6
Chromosome : CHR 5: 151,157,881-151,100,705
Locus : 5q33.1
This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq, Jul 2008]
Gene Symbol : UTRN
Gene Name : Utrophin
Chromosome : CHR 6: 144,284,954-144,853,033
Locus : 6q24.2
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