TMPRSS3 (NM_032401) Human Tagged ORF Clone

CAT#: RC224957L4

  • LentiORF®

Lenti ORF clone of Human transmembrane protease, serine 3 (TMPRSS3), transcript variant B, mGFP tagged


  "NM_032401" in other vectors (4)

Reconstitution Protocol

USD 620.00

3 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Tagged ORF Clone
Tag mGFP
Symbol TMPRSS3
Synonyms DFNB8; DFNB8, DFNB10, ECHOS1, TADG12; DFNB10; ECHOS1; OTTHUMP00000109345; serine protease TADG12; TADG12; transmembrane protease, serine 3
Vector pLenti-C-mGFP-P2A-Puro
E. coli Selection Chloramphenicol (34 ug/mL)
Mammalian Cell Selection Puromycin
Sequence Data
The ORF insert of this clone is exactly the same as(RC224957).
Restriction Sites SgfI-MluI      Cloning Scheme for this gene     
ACCN NM_032401
ORF Size 981 bp
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_032401.1, NP_115777.1
RefSeq Size 2554
RefSeq ORF 983
Locus ID 64699
Domains Tryp_SPc
Protein Families Druggable Genome, Protease, Transmembrane
MW 36.2 kDa
Gene Summary This gene encodes a protein that belongs to the serine protease family. The encoded protein contains a serine protease domain, a transmembrane domain, an LDL receptor-like domain, and a scavenger receptor cysteine-rich domain. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified by its association with both congenital and childhood onset autosomal recessive deafness. This gene is expressed in fetal cochlea and many other tissues, and is thought to be involved in the development and maintenance of the inner ear or the contents of the perilymph and endolymph. This gene was also identified as a tumor-associated gene that is overexpressed in ovarian tumors. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]

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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.