Col11a2 (NM_009926) Mouse Tagged ORF Clone Lentiviral Particle

CAT#: MR220599L4V

  • LentiORF®

Lenti ORF particles, Col11a2 (GFP-tagged) - Mouse collagen, type XI, alpha 2 (Col11a2), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 25,080.00


货期*
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规格
    • 200 ul

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Specifications

Product Data
Product Name Col11a2 (NM_009926) Mouse Tagged ORF Clone Lentiviral Particle
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_009926
ORF Size 4950 bp
Sequence Data
The ORF insert of this clone is exactly the same as(MR220599).
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_009926.1, NP_034056.1
RefSeq Size 5605 bp
RefSeq ORF 4953 bp
Locus ID 12815
Gene Summary This gene encodes the alpha-2 subunit of type XI collagen, one of the low abundance fibrillar collagens found in cartilage. The encoded protein, in association with other collagen subunits, forms a heterotrimeric type XI procollagen that may undergo proteolytic processing similar to the alpha-1 subunit. Mice lacking the encoded protein exhibit a mild phenotype similar to nonocular Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED) as well as a nonsyndromic form of deafness called DFNA13. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]
*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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