SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
TSPAN9-DNM1L-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
TSPAN9-DNM1L-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
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
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. Alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq, Nov 2009]
Gene Symbol : TSPAN9
Gene Name : Tetraspanin 9
Chromosome : CHR 12: 307,735,4-328,656,3
Locus : 12p13.33-p13.32
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