| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ASAH1-DDX21-20-RERE | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-REOR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-REGO | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-REGR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-REAQ | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-ORRE | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-OROR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-ORGO | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-ORGR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-ORAQ | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GORE | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GOOR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GOGO | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GOGR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GOAQ | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GRRE | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GROR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GRGO | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GRGR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-GRAQ | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-AQRE | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-AQOR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-AQGO | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-AQGR | 20 (40 μL) | 200 μL |
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| ASAH1-DDX21-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a member of the acid ceramidase family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. Processing of this preproprotein generates alpha and beta subunits that heterodimerize to form the mature lysosomal enzyme, which catalyzes the degradation of ceramide into sphingosine and free fatty acid. This enzyme is overexpressed in multiple human cancers and may play a role in cancer progression. Mutations in this gene are associated with the lysosomal storage disorder, Farber lipogranulomatosis, and a neuromuscular disorder, spinal muscular atrophy with progressive myoclonic epilepsy. [provided by RefSeq, Oct 2015]
Gene Symbol : ASAH1
Gene Name : N-acylsphingosine amidohydrolase 1
Chromosome : CHR 8: 180,849,97-180,562,98
Locus : 8p22
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an antigen recognized by autoimmune antibodies from a patient with watermelon stomach disease. This protein unwinds double-stranded RNA, folds single-stranded RNA, and may play important roles in ribosomal RNA biogenesis, RNA editing, RNA transport, and general transcription. [provided by RefSeq, Jul 2008]
Gene Symbol : DDX21
Gene Name : DExD-box helicase 21
Chromosome : CHR 10: 689,561,22-689,850,68
Locus : 10q22.1
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