SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
ATP2A2-COL2A1-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
ATP2A2-COL2A1-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol into the sarcoplasmic reticulum lumen, and is involved in regulation of the contraction/relaxation cycle. Mutations in this gene cause Darier-White disease, also known as keratosis follicularis, an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and abnormal keratinization. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2008]
Gene Symbol : ATP2A2
Gene Name : ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2
Chromosome : CHR 12: 110,281,226-110,351,092
Locus : 12q24.11
This gene encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : COL2A1
Gene Name : Collagen type II alpha 1 chain
Chromosome : CHR 12: 480,062,11-479,729,64
Locus : 12q13.11
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