| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| VIM-DNM1L-20-RERE | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-REOR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-REGO | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-REGR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-REAQ | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-ORRE | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-OROR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-ORGO | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-ORGR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-ORAQ | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GORE | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GOOR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GOGO | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GOGR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GOAQ | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GRRE | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GROR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GRGO | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GRGR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-GRAQ | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-AQRE | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-AQOR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-AQGO | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-AQGR | 20 (40 μL) | 200 μL |
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| VIM-DNM1L-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a type III intermediate filament protein. Intermediate filaments, along with microtubules and actin microfilaments, make up the cytoskeleton. The encoded protein is responsible for maintaining cell shape and integrity of the cytoplasm, and stabilizing cytoskeletal interactions. This protein is involved in neuritogenesis and cholesterol transport and functions as an organizer of a number of other critical proteins involved in cell attachment, migration, and signaling. Bacterial and viral pathogens have been shown to attach to this protein on the host cell surface. Mutations in this gene are associated with congenital cataracts in human patients. [provided by RefSeq, Aug 2017]
Gene Symbol : VIM
Gene Name : Vimentin
Chromosome : CHR 10: 172,279,34-172,375,92
Locus : 10p13
This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]
Gene Symbol : DNM1L
Gene Name : Dynamin 1 like
Chromosome : CHR 12: 326,791,99-327,456,49
Locus : 12p11.21
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Lorem Ipsum is simply dummy text of the printing and typesetting industry.