EFEMP2 (NM_016938) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC203726L2V

  • LentiORF®

Lenti ORF particles, EFEMP2 (mGFP-tagged) - Human EGF containing fibulin-like extracellular matrix protein 2 (EFEMP2), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK DDK w/ Puro mGFP mGFP w/ Puro

AAV Particle: DDK


Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 1,007.00

7 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol EFEMP2
Synonyms ARCL1B; FBLN4; MBP1; UPH1
Mammalian Cell Selection None
Vector pLenti-C-mGFP
ACCN NM_016938
ORF Size 1329 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC203726).
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_016938.2
RefSeq Size 2096 bp
RefSeq ORF 1332 bp
Locus ID 30008
UniProt ID O95967
Cytogenetics 11q13.1
Domains EGF_CA, EGF, EGF
Protein Families Druggable Genome, Secreted Protein
MW 49.4 kDa
Gene Summary A large number of extracellular matrix proteins have been found to contain variations of the epidermal growth factor (EGF) domain and have been implicated in functions as diverse as blood coagulation, activation of complement and determination of cell fate during development. The protein encoded by this gene contains four EGF2 domains and six calcium-binding EGF2 domains. This gene is necessary for elastic fiber formation and connective tissue development. Defects in this gene are cause of an autosomal recessive cutis laxa syndrome. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jan 2011]

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*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.