ADAMTS18 (NM_199355) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC209192L3V
- LentiORF®
Lenti ORF particles, ADAMTS18 (Myc-DDK tagged) - Human ADAM metallopeptidase with thrombospondin type 1 motif, 18 (ADAMTS18), 200ul, >10^7 TU/mL
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CNY 11,210.00
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Specifications
Product Data | |
Product Name | ADAMTS18 (NM_199355) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | ADAMTS21; KNO2; MMCAT |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_199355 |
ORF Size | 3663 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC209192).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_199355.1 |
RefSeq Size | 5510 bp |
RefSeq ORF | 3666 bp |
Locus ID | 170692 |
Protein Families | Protease, Secreted Protein |
MW | 135 kDa |
Gene Summary | This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may regulate hemostatic balance and function as a tumor suppressor. Mutations in this gene may be associated with microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) and cone-rod dystrophy in human patients. [provided by RefSeq, May 2016] |
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