SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
TMC6-DNAH17-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
TMC6-DNAH17-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
Dyneins are microtubule-associated motor protein complexes composed of several heavy, light, and intermediate chains. DNAH17 is a heavy chain associated with axonemal dynein (Milisav and Affara, 1998 [PubMed 9545504]).[supplied by OMIM, Mar 2008]
Gene Symbol : DNAH17
Gene Name : Dynein axonemal heavy chain 17
Chromosome : CHR 17: 785,774,29-784,236,96
Locus : 17q25.3
Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25.3. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane channels. This gene encodes a transmembrane channel-like protein with 10 transmembrane domains and 2 leucine zipper motifs. [provided by RefSeq, Jul 2008]
Gene Symbol : TMC6
Gene Name : Transmembrane channel like 6
Chromosome : CHR 17: 781,324,26-781,087,74
Locus : 17q25.3
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Lorem Ipsum is simply dummy text of the printing and typesetting industry.