OriGene Logo

Customer Login

Checkout as a new customer

Creating an account has many benefits:

  • See order and shipping status
  • Track order history
  • Check out faster
Create an Account

PDE4DIP Human shRNA Plasmid Kit (Locus ID 9659)

Be the first to review this product
SKU
TL310543
PDE4DIP - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
  $1,013.00
2 Weeks*

Frequently Bought Together (4)

TA366480 PDE4DIP rabbit polyclonal antibody
100 ul
$310.00
EB200002 Lateral flow testing sticks used for the semi-quantitative detection of the lentiviral p24 protein, 20 tests
20 Tests
$450.00
TR30037 Lenti-vpak packaging kit - packaging plasmids and transfection reagent
10 reactions
$720.00
TF81001 TurboFectin Transfection Reagent (1 mL in 1 vial)
1 ml in 1 vial
$530.00

Other products for "PDE4DIP or NM_001002810"

Specifications
Specifications
Product Data
Locus ID 9659
Synonyms CMYA2; MMGL
Vector pGFP-C-shLenti
E. coli Selection Chloramphenicol (34 ug/ml)
Mammalian Cell Selection Puromycin
Format Lentiviral plasmids
Components PDE4DIP - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 9659). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free.
RefSeq BC005949, NM_001002810, NM_001002811, NM_001002812, NM_001195260, NM_001195261, NM_001198832, NM_001198834, NM_014644, NM_022359, NM_001350520, NM_001350521, NM_001350522, NM_001350523, NM_001002810.1, NM_001002810.2, NM_001002810.3, NM_014644.1, NM_014644.2, NM_014644.3, NM_014644.4, NM_014644.5, NM_001002812.1, NM_001002812.2, NM_001002811.1, NM_001002811.2, NM_022359.3, NM_022359.4, NM_022359.5, NM_001195260.1, NM_001195261.1, NM_001198832.1, NM_001198832.2, NM_001198834.1, NM_001198834.2, NM_001198834.3, BC004860, BC025406, BC078660, BC132717, BC152439, BC152553, BC172441, NM_001002810.4, NM_022359.7, NM_001002812.3
UniProt ID Q5VU43
Summary The protein encoded by this gene serves to anchor phosphodiesterase 4D to the Golgi/centrosome region of the cell. Defects in this gene may be a cause of myeloproliferative disorder (MBD) associated with eosinophilia. Several transcript variants encoding different isoforms have been found for this gene. provided by RefSeq, Aug 2010
shRNA Design These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact techsupport@origene.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service.
Storage Store at -20°C
Shipping Ambient
Reviews
Write Review
 
 
 
 
 

Be the first to review this product

Please note:
Only reviews with images are eligible for a $20/20€ Amazon gift card.
Reviews without images are eligible for a $10/10€ Amazon gift card.
For more details about the terms and conditions, please visit the promotion page.

Review image
Documents
Resources

file-alt Citations

*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.

Related Products