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LipoKnoxa™ Human LZTFL1 shRNA Ad5 Particle (Silencing)
Cat. No.:
V0126XX73
Species:
Human
Target Gene:
LZTFL1
Vector System:
Adenovirus
Modulation Type:
Silencing (shRNA)
SPECIFIC INQUIRY
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| Sub Cat. No. | TargetSeq | Region | Inquiry |
|---|---|---|---|
| V0126XX73-1 | TTAGAACTAGAGTTCCTATTT | 3' UTR | Inquiry |
| V0126XX73-2 | TGGAACAGCAGAACTCCTAAA | CDS | Inquiry |
| V0126XX73-3 | GCCTATACCAATGTGTTACTT | CDS | Inquiry |
| V0126XX73-4 | Other | Inquiry |
Product Overview
Description:
LipoKnoxa™ Human LZTFL1 shRNA Ad5 Particle (Silencing) provides an efficient method to silence LZTFL1, a key regulator of BBSome ciliary trafficking. Deficiency in LZTFL1 is linked to Bardet-Biedl Syndrome and disrupted satiety signaling. Through high-efficiency Ad5 delivery of optimized shRNA (U6 or miR30), researchers can explore the intersection of ciliary protein sorting and weight regulation. We ensure experimental safety and data integrity through comprehensive QC, including functional titer assays and negative results for sterility and mycoplasma.
Production Cell Line:
HEK293
Viral Backbone:
Adenovirus type 5 (dE1/E3)
Promoter:
U6; CMV; EF1α; CAG; UBC
Product Availability:
Produced Upon Order
Specification
Titer Test:
qPCR
Insert Verification:
All viral preparations are validated via Sequencing and PCR to ensure 100% sequence identity and the structural integrity of the vector genomes.
Sterility Test:
This product has been certified sterile following comprehensive microbial growth analysis, confirming the absence of bacterial and fungal contamination.
Mycoplasma Test:
This product was certified negative for mycoplasma contamination following stringent QC analysis, ensuring the absence of all mycoplasmal agents.
Other QC:
Beyond standard protocols, we offer customized knockdown efficiency validation through in vitro and in vivo assessments. This includes precise analysis of mRNA/protein reduction and subsequent biological responses to ensure the functional potency of the shRNA-mediated gene silencing.
Storage:
Upon receipt, viral preparations should be immediately transferred to -80°C for long-term storage to ensure maximum stability and maintain product integrity.
Stability:
This product maintains excellent biological activity for 6–12 months (and up to 2 years in specific cases) when stored continuously at -80°C. Once thawed, the working solution remains stable for 2–3 weeks at 4°C without significant loss of viral potency.
Shipping Condition:
All viral preparations are shipped on dry ice to ensure maximum biological activity and stability during transit.
Handling Notes:
Viral particles are susceptible to temperature fluctuations and freeze-thaw cycles. To preserve functional titers, it is essential to aliquot the vector into low-protein-binding tubes immediately upon first thaw. To ensure experimental success and biological safety, all procedures must be conducted within a certified biosafety cabinet.
Intended Use:
This product is intended for research use only and is not for use in diagnosis or therapeutic applications.
Product Disclaimer:
While our products are committed to excellence through rigorous internal QC inspections, we cannot guarantee specific performance or experimental outcomes due to the inherent complexity of biological systems. Users assume full responsibility for product storage, handling, and strict compliance with all applicable safety protocols, biosafety requirements, and legal regulations during all operational processes.
Target Profile
Gene Name:
LZTFL1
Full Name:
Leucine zipper transcription factor like 1
Gene Symbol:
BBS17
Gene ID:
54585
RefSeq ID-1:
NP_001263307.1
RefSeq ID-2:
NM_001276378.2
Summary:
LZTFL1 encodes a cytoplasmic protein that interacts with Bardet–Biedl syndrome (BBS) proteins to regulate the trafficking of proteins to the ciliary membrane. Loss-of-function mutations cause a form of BBS characterized by polydactyly, obesity, hypogonadism, and cognitive impairment. LZTFL1 may also act as a tumor suppressor through interactions with E-cadherin and the actin cytoskeleton, influencing epithelial-to-mesenchymal transitions.
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