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 UBC promoter, 25 ul each, functional titer of 1x10^8 TU/ml
$980.00
HSH-217696-100
Lentiviral human HSPG2 shRNA (UBC) (100)
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, 4x25 ul each, functional titer of 1x10^8 TU/ml
$2,190.00
HSH-217696-10ug
Lentiviral human HSPG2 shRNA (UBC) plasmid
Lentiviral constructs for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, 10 ug each
$1,290.00
HSH-217696-25GFP
Lentiviral human HSPG2 shRNA (UBC,GFP) (25)
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a GFP reporter, 25 ul each, functional titer of 1x10^8 TU/ml
$980.00
HSH-217696-100GFP
Lentiviral human HSPG2 shRNA (UBC,GFP) (100)
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a GFP reporter, 4x25 ul each, functional titer of 1x10^8 TU/ml
$2,190.00
HSH-217696-10ugGFP
Lentiviral human HSPG2 shRNA (UBC,GFP) plasmid
Lentiviral constructs for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a GFP reporter, 10 ug each
$1,290.00
HSH-217696-25RFP
Lentiviral human HSPG2 shRNA (UBC,RFP) (25)
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a RFP reporter, 25 ul each, functional titer of 1x10^8 TU/ml
$980.00
HSH-217696-100RFP
Lentiviral human HSPG2 shRNA (UBC,RFP) (100)
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a RFP reporter, 4x25 ul each, functional titer of 1x10^8 TU/ml
$2,190.00
HSH-217696-10ugRFP
Lentiviral human HSPG2 shRNA (UBC,RFP) plasmid
Lentiviral constructs for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a RFP reporter, 10 ug each
$1,290.00
HSH-217696-25iRFP
Lentiviral human HSPG2 shRNA (UBC,iRFP) (25)
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a miRFP670 reporter, 25 ul each, functional titer of 1x10^8 TU/ml
$980.00
HSH-217696-100iRFP
Lentiviral human HSPG2 shRNA (UBC,iRFP) (100)
Lentiviral particles for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a miRFP670 reporter, 4x25 ul each, functional titer of 1x10^8 TU/ml
$2,190.00
HSH-217696-10ugiRFP
Lentiviral human HSPG2 shRNA (UBC,iRFP) plasmid
Lentiviral constructs for 3 unique target specific shRNA and 1 scramble shRNA driven by the UBC promoter, with a miRFP670 reporter, 10 ug each
$1,290.00
Product Details
Target gene information
Gene symbol
HSPG2
Synonyms
HSPG PLC PRCAN SJA SJS SJS1
Species
human
Gene ID
3339
Summary
This gene encodes the perlecan protein, which consists of a core protein to which three long chains of glycosaminoglycans (heparan sulfate or chondroitin sulfate) are attached. The perlecan protein is a large multidomain proteoglycan that binds to and cross-links many extracellular matrix components and cell-surface molecules. It has been shown that this protein interacts with laminin, prolargin, collagen type IV, FGFBP1, FBLN2, FGF7 and transthyretin, etc., and it plays essential roles in multiple biological activities. Perlecan is a key component of the vascular extracellular matrix, where it helps to maintain the endothelial barrier function. It is a potent inhibitor of smooth muscle cell proliferation and is thus thought to help maintain vascular homeostasis. It can also promote growth factor (e.g., FGF2) activity and thus stimulate endothelial growth and re-generation. It is a major component of basement membranes, where it is involved in the stabilization of other molecules as well as being involved with glomerular permeability to macromolecules and cell adhesion. Mutations in this gene cause Schwartz-Jampel syndrome type 1, Silverman-Handmaker type of dyssegmental dysplasia, and tardive dyskinesia. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014].
