ADAMTSL2 (NM_014694) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC208512L3V

  • LentiORF®

Lenti ORF particles, ADAMTSL2 (Myc-DDK-tagged)-Human ADAMTS-like 2 (ADAMTSL2), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 8,930.00


货期*
详询

规格
    • 200 ul

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Specifications

Product Data
Product Name ADAMTSL2 (NM_014694) Human Tagged ORF Clone Lentiviral Particle
Synonyms ADAMTSL-2; GPHYSD1
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_014694
ORF Size 2853 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC208512).
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_014694.3
RefSeq Size 3740 bp
RefSeq ORF 2856 bp
Locus ID 9719
Domains tsp_1
Protein Families Secreted Protein
MW 104.6 kDa
Gene Summary This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) and ADAMTS-like protein family. Members of the family 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 protein encoded by this gene lacks the protease domain, and is therefore of a member of the the ADAMTS-like protein subfamily. It is a secreted glycoprotein that binds the cell surface and extracellular matrix; it also interacts with latent transforming growth factor beta binding protein 1. Mutations in this gene have been associated with geleophysic dysplasia. [provided by RefSeq, Feb 2009]
*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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