| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| USP48-KALRN-20-RERE | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-REOR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-REGO | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-REGR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-REAQ | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-ORRE | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-OROR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-ORGO | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-ORGR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-ORAQ | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GORE | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GOOR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GOGO | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GOGR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GOAQ | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GRRE | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GROR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GRGO | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GRGR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-GRAQ | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-AQRE | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-AQOR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-AQGO | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-AQGR | 20 (40 μL) | 200 μL |
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| USP48-KALRN-20-AQAQ | 20 (40 μL) | 200 μL |
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Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016]
Gene Symbol : KALRN
Gene Name : Kalirin RhoGEF kinase
Chromosome : CHR 3: 124,033,340-124,726,324
Locus : 3q21.1-q21.2
This gene encodes a protein containing domains that associate it with the peptidase family C19, also known as family 2 of ubiquitin carboxyl-terminal hydrolases. Family members function as deubiquitinating enzymes, recognizing and hydrolyzing the peptide bond at the C-terminal glycine of ubiquitin. Enzymes in peptidase family C19 are involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Gene Symbol : USP48
Gene Name : Ubiquitin specific peptidase 48
Chromosome : CHR 1: 217,836,19-216,782,97
Locus : 1p36.12
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