pGFP-A-shAAV shRNA Vector

SKU
TR30034
HuSH shRNA GFP AAV Cloning Vector (pGFP-A-shAAV Vector), 5 ug
  $880.00
In Stock*
Specifications
Specifications
Product Data
Control Type Negative
Fluorescent Label GFP
Mammalian Cell Selection Puromycin
Viral Packaging Adeno-associated virus (AAV)
Features
  • The pGFP-A-shAAV vector was created with an integrated turboGFP element to readily verify transfection efficiency
  • It incorporates both a ampicillin and puromycin resistance elements for greater selection capabilities.
  • The AAV2-backbone vector enables the helper-free packaging method to produce AAV particles.
  • U6_F Primer can be used to sequence the target sequence after cloning.
Download Vector Sequence
Components 1 vial of 5 ug lyophilized pGFP-A-shAAV shRNA cloning vector
Quality Control This vector was sequence verified and functionally validated.
Storage Store the vector DNA at -20°C.
Stability Vector DNA is stable for at least one year from date of receipt when stored at -20°C.
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Documents
Resources

file-alt Citations

Male rat hypothalamic extraretinal photoreceptor Opsin3 is sensitive to osmotic stimuli and light
Bárez-López, Bishop, Searby et al
J Neuroendocrinol (2024)
Cited by 7
AI Summary: OriGene's HuSH shRNA GFP AAV Cloning Vector (pGFP-A-shAAV Vector; TR30034) was used to clone Opn3-specific and control shRNAs, enabling the researchers to investigate the functional role of Opn3 in hypothalamic neurons by modulating its expression.
Snippet: A Opn3 short hairpin RNA (shRNA) (GGGACAGGCCAAAGAAGAAAG) and a non-targeting shRNA sequence (AATTCTCCGAACGTGTCACGT),23 used as a control, were cloned into HuSH shRNA GFP AAV Cloning Vector (pGFP-A-shAAV Vector;TR30034, Origene). The efficiency of the specific Opn3 shRNA was tested in HEK293T/17 cells (human embryonic kidney cell line, CRL-11268, ATCC) transiently overexpressing rat Opn3. …
Transcription factor Creb3l1 maintains proteostasis in neuroendocrine cells
Greenwood, Gillard, Farrukh et al
Mol Metab (2022) 63, 101542 DOI: 10.1016/j.molmet.2022.101542
Cited by 16
AI Summary: OriGene’s pGFP-A-shAAV vector (TR30034) was used in this study to clone Creb3l1 and non-targeting shRNAs for generating adeno-associated viruses (AAVs), enabling targeted knockdown and functional analysis of Creb3l1 in neuroendocrine cells.
Snippet: (1 ng/well, Promega, E2261). Samples were collected 48 h post transfection. 2.7 Virus production and validation Creb3l1 and non-targeting short hairpin RNAs (shRNAs) were cloned into pGFP-A-shAAV (OriGene, TR30034) as previously described [20]. We generated adeno-associated viruses (AAVs) expressing GFP and Creb3l1CA directed by a 2 kb fragment of the rat Avp promoter. AAV particles (AAV1/2) w
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Dyrk1b promotes hepatic lipogenesis by bypassing canonical insulin signaling and directly activating mTORC2 in mice
Bhat, Narayanan, Fathzadeh et al
J Clin Invest (2021) 132 (3) DOI: 10.1172/JCI153724
AI Summary: OriGene products contributed to this study by providing plasmids containing scrambled shRNA and four Dyrk1b shRNAs (Catalog # TL514285) as well as the AAV vector with U6 promoter and inverse terminal repeats (Catalog # TR30034), which were used to manipulate Dyrk1b expression in mouse liver for functional analysis.
Snippet: … Dyrk1b AAV-shRNA production. The plasmids containing scrambled shRNA and 4 Dyrk1b shRNAs were purchased from Origene Inc. (catalog TL514285) and shuttled into the AAV vector with U6 promoter and inverse terminal repeats (Origene Inc., TR30034). The sequences of the Dyrk1b shRNAs and scrambled shRNA are repor;Dyrk1b AAV-shRNA production: The plasmids containin scrambled shRNA and four Dyrk1b 11 shRNAs was purchased from Origene Inc. (Catalog # TL514285) and shuttled into the AAV vector 12 with U6 promoter and Inverse terminal repeats, (Origene Inc., Catalog # TR30034). The 13 sequences of the Dyrk1b shRNAs and scrambled shRNA are reported in STable2. …
Rapid 3D Enhanced Resolution Microscopy Reveals Diversity in Dendritic Spinule Dynamics, Regulation, and Function
Zaccard, Shapiro, Martin-de-Saavedra et al
Neuron (2020) 107 (3), 522-537.e6 DOI: 10.1016/j.neuron.2020.04.025
Cited by 46
AI Summary: OriGene’s pGFP-A-shAAV plasmid (Cat#TR30034) was used in this study to manipulate gene expression in neurons, enabling the investigation of dendritic spinule dynamics and regulatory mechanisms.
Snippet: Skip to article;pGFP-A-shAAV Origene Cat#TR30034 pLV-Kal-7 mCherry [NM_001164268.1] VectorBuilder VB181102-1224vxt
Transcription factor Creb3l1 regulates the synthesis of prohormone convertase enzyme PC1/3 in endocrine cells
Greenwood, Paterson, Rahman et al
J. Neuroendocrinol. (2020) 32 (4), e12851 DOI: 10.1111/jne.12851
Cited by 27
AI Summary: OriGene’s pGFP-A-shAAV vector was used to clone Creb3l1 and non-targeting shRNAs, enabling the generation of viral constructs for manipulating Creb3l1 expression in vivo to study its regulatory effect on PC1/3 synthesis in endocrine cells.
Snippet: Introduction of viral vectors into the SON The Creb3l1 and non-targeting short hairpin RNAs (shRNAs, supplemental table 1) were cloned into pGFP-A-shAAV (ORIGENE). Adeno-associated viral particles (AAV1/2) were produced using a helper;- Introduction of viral vectors into the SON The Creb3l1 and non-targeting short hairpin RNAs (shRNAs, supplemental table 1) were cloned into pGFP-A-shAAV (ORIGENE). …
Showing 1-5 of 5 papers.
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