COG8 (NM_032382) Human Untagged Clone
$300.00
4 Weeks*
Specifications
| Product Data | |
| Type | Human Untagged Clone |
|---|---|
| Target Symbol | COG8 |
| Synonyms | CDG2H; DOR1 |
| Vector | pCMV6-XL5 |
| E. coli Selection | Ampicillin (100 ug/mL) |
| Mammalian Cell Selection | None |
| Sequence Data | |
| Restriction Sites | NotI-NotI | |
| ACCN | NM_032382 |
| Insert Size | 1750 bp |
| OTI Disclaimer | Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP). |
| Components | The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water). |
| Reconstitution Method | 1. Centrifuge at 5,000xg for 5min. 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA. 3. Close the tube and incubate for 10 minutes at room temperature. 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom. 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C. |
| Note | Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required. |
| Shipping | Ambient |
| Reference Data | |
| RefSeq | NM_032382.1, NP_115758.1 |
| RefSeq Size | 2522 bp |
| RefSeq ORF | 660 bp |
| Locus ID | 84342 |
| UniProt ID | Q96MW5 |
| Cytogenetics | 16q22.1 |
| Domains | Dor1 |
| Protein Families | Druggable Genome |
| Summary | This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. provided by RefSeq, Jul 2008 |
Reviews
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
"NM_032382" in other vectors (5)
| SKU | Description | Size | Price | |
|---|---|---|---|---|
| RC219727 | COG8 (Myc-DDK-tagged)-Human component of oligomeric golgi complex 8 (COG8) | 10 ug |
$570.00
|
|
| RC219727L3 | Lenti ORF clone of Human component of oligomeric golgi complex 8 (COG8), Myc-DDK-tagged | 10 ug |
$870.00
|
|
| RC219727L4 | Lenti ORF clone of Human component of oligomeric golgi complex 8 (COG8), mGFP tagged | 10 ug |
$870.00
|
|
| RG219727 | COG8 (tGFP-tagged) - Human component of oligomeric golgi complex 8 (COG8) | 10 ug |
$770.00
|
|
| SC318048 | COG8 (untagged)-Human component of oligomeric golgi complex 8 (COG8) | 10 ug |
$628.00
|
|
Citations
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen
complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
in shipping.
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