MOCS1 Human shRNA Plasmid Kit (Locus ID 4337)

Specifications

Product Data
Product Name	MOCS1 Human shRNA Plasmid Kit (Locus ID 4337)
Locus ID	4337
UniProt ID	Q9NZB8
Synonyms	MIG11; MOCOD; MOCS1A; MOCS1B
Vector	pGFP-C-shLenti
Format	Lentiviral plasmids
Kit Components	MOCS1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 4337). 5µg purified plasmid DNA per construct 29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free.
RefSeq	NM_001075098, NM_005942, NM_005943, NM_138928, NR_033233, NM_001358529, NM_001358530, NM_001358531, NM_001358533, NM_001358534, NM_001075098.1, NM_001075098.2, NM_001075098.3, NM_005943.2, NM_005943.3, NM_005943.4, NM_005943.5, NM_138928.1, NM_005942.1, BC036839, BC140421, NM_001075098.4
Summary	Molybdenum cofactor biosynthesis is a conserved pathway leading to the biological activation of molybdenum. The protein encoded by this gene is involved in this pathway. This gene was originally thought to produce a bicistronic mRNA with the potential to produce two proteins (MOCS1A and MOCS1B) from adjacent open reading frames. However, only the first open reading frame (MOCS1A) has been found to encode a protein from the putative bicistronic mRNA, whereas additional splice variants are likely to produce a fusion between the two open reading frames. This gene is defective in patients with molybdenum cofactor deficiency, type A. A related pseudogene has been identified on chromosome 16. [provided by RefSeq, Nov 2017]
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).

*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.