SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
AGAP2-TMEM67-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
AGAP2-TMEM67-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]
Gene Symbol : TMEM67
Gene Name : Transmembrane protein 67
Chromosome : CHR 8: 937,548,43-938,326,52
Locus : 8q22.1
The protein encoded by this gene belongs to the centaurin gamma-like family. It mediates anti-apoptotic effects of nerve growth factor by activating nuclear phosphoinositide 3-kinase. It is overexpressed in cancer cells, and promotes cancer cell invasion. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]
Gene Symbol : AGAP2
Gene Name : ArfGAP with GTPase domain, ankyrin repeat and PH domain 2
Chromosome : CHR 12: 577,422,00-577,237,64
Locus : 12q14.1
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