SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
AQP1-CFB-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
AQP1-CFB-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a small integral membrane protein with six bilayer spanning domains that functions as a water channel protein. This protein permits passive transport of water along an osmotic gradient. This gene is a possible candidate for disorders involving imbalance in ocular fluid movement. [provided by RefSeq, Aug 2016]
Gene Symbol : AQP1
Gene Name : Aquaporin 1 (Colton blood group)
Chromosome : CHR 7: 309,117,99-309,255,15
Locus : 7p14.3
This gene encodes complement factor B, a component of the alternative pathway of complement activation. Factor B circulates in the blood as a single chain polypeptide. Upon activation of the alternative pathway, it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. This cluster includes several genes involved in regulation of the immune reaction. Polymorphisms in this gene are associated with a reduced risk of age-related macular degeneration. The polyadenylation site of this gene is 421 bp from the 5' end of the gene for complement component 2. [provided by RefSeq, Jul 2008]
Gene Symbol : CFB
Gene Name : Complement factor B
Chromosome : CHR 6: 319,459,43-319,520,83
Locus : 6p21.33
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