SLC10A1 Human shRNA Plasmid Kit (Locus ID 6554)
CAT#: TL309420
SLC10A1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
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CNY 5,740.00
Cited in 1 publication. |
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CNY 4,070.00
Specifications
Product Data | |
Product Name | SLC10A1 Human shRNA Plasmid Kit (Locus ID 6554) |
Locus ID | 6554 |
UniProt ID | Q14973 |
Synonyms | FHCA2; NTCP |
Vector | pGFP-C-shLenti |
Format | Lentiviral plasmids |
Kit Components | SLC10A1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 6554). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
RefSeq | NM_003049, NM_003049.1, NM_003049.2, NM_003049.3, BC069799, BC069822, BC074724, BC126298, BC136355, NM_003049.4 |
Summary | The protein encoded by this gene belongs to the sodium/bile acid cotransporter family, which are integral membrane glycoproteins that participate in the enterohepatic circulation of bile acids. Two homologous transporters are involved in the reabsorption of bile acids; the ileal sodium/bile acid cotransporter with an apical cell localization that absorbs bile acids from the intestinal lumen, bile duct and kidney, and the liver-specific sodium/bile acid cotransporter, represented by this protein, that is found in the basolateral membranes of hepatocytes. Bile acids are the catabolic product of cholesterol metabolism, hence this protein is important for cholesterol homeostasis. [provided by RefSeq, Oct 2011] |
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. |
Performance Guaranteed | OriGene guarantees that the sequences in the shRNA expression cassettes are verified to correspond to the target gene with 100% identity. One of the four constructs at minimum are guaranteed to produce 70% or more gene expression knock-down provided a minimum transfection efficiency of 80% is achieved. Western Blot data is recommended over qPCR to evaluate the silencing effect of the shRNA constructs 72 hrs post transfection. To properly assess knockdown, the gene expression level from the included scramble control vector must be used in comparison with the target-specific shRNA transfected samples. For non-conforming shRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the shRNA kit. To arrange for a free replacement with newly designed constructs, please contact Technical Services at techsupport@origene.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled shRNA control (Western Blot data preferred). |
Citations (1)
The use of this RNAi has been cited in the following citations: |
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N-linked glycosylation is not essential for sodium taurocholate cotransporting polypeptide to mediate hepatitis B virus infection in vitro
,Lee, J;Zong, L;Krotow, A;Qin, Y;Jia, L;Zhang, J;Tong, S;Li, J;,
J. Virol.
,PubMed ID 29793953
[SLC10A1]
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