KIRREL 3 (KIRREL3) (NM_032531) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC211025L2V

  • LentiORF®

Lenti ORF particles, KIRREL3 (mGFP-tagged) - Human kin of IRRE like 3 (Drosophila) (KIRREL3), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

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


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

USD 1,262.00

7 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol KIRREL 3
Synonyms KIRRE; MRD4; NEPH2; PRO4502
Mammalian Cell Selection None
Vector pLenti-C-mGFP
ACCN NM_032531
ORF Size 2334 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC211025).
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_032531.2
RefSeq Size 3794 bp
RefSeq ORF 2337 bp
Locus ID 84623
UniProt ID Q8IZU9
Cytogenetics 11q24.2
Protein Families Transmembrane
MW 85.3 kDa
Gene Summary The protein encoded by this gene is a member of the nephrin-like protein family. These proteins are expressed in fetal and adult brain, and also in podocytes of kidney glomeruli. The cytoplasmic domains of these proteins interact with the C-terminus of podocin, also expressed in the podocytes, cells involved in ensuring size- and charge-selective ultrafiltration. The protein encoded by this gene is a synaptic cell adhesion molecule with multiple extracellular immunoglobulin-like domains and a cytoplasmic PDZ domain-binding motif. Mutations in this gene are associated with several neurological and cognitive disorders. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]

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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.