Lentiviral particles or plasmids for 3 unique target specific shRNA and 1 scramble shRNA, RT-PCR primer mix for target specific gene and a housekeeping gene
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the CAG promoter, 25 ul each, functional titer of 1x10^8 TU/ml
$980.00
MSH-621650-100
Lentiviral mouse D130043K22Rik shRNA (CAG) (100)
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the CAG promoter, 4x25 ul each, functional titer of 1x10^8 TU/ml
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the CAG promoter, with a GFP reporter, 25 ul each, functional titer of 1x10^8 TU/ml
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the CAG promoter, with a GFP reporter, 4x25 ul each, functional titer of 1x10^8 TU/ml
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the CAG promoter, with a RFP reporter, 25 ul each, functional titer of 1x10^8 TU/ml
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by CAG promoter, with a RFP reporter, 4x25 ul each, functional titer of 1x10^8 TU/ml
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the CAG promoter, with a miRFP670 reporter, 25 ul each, functional titer of 1x10^8 TU/ml
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the CAG promoter, with a miRFP670 reporter, 4x25 ul each, functional titer of 1x10^8 TU/ml
Lentiviral constructs for 3 unique target specific shRNA and 1 scramble shRNA driven by the CAG promoter, with a miRFP670 reporter, 10 ug each
$1,290.00
Product Details
Target gene information
Gene symbol
D130043K22Rik
Synonyms
4930451E12Rik Kiaa0319
Species
mouse
Gene ID
210108
Summary
This gene encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. The encoded protein may play a role in the development of the cerebral cortex by regulating neuronal migration and cell adhesion. Single nucleotide polymorphisms in a similar gene in human are associated with dyslexia. Alternatively spliced transcript variants have been identifed. [provided by RefSeq, May 2015].
