TRIM37 Human shRNA Plasmid Kit (Locus ID 4591)
CAT#: TR308645
TRIM37 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
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CNY 6,790.00
货期*
2周
规格
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Specifications
Product Data | |
Product Name | TRIM37 Human shRNA Plasmid Kit (Locus ID 4591) |
Locus ID | 4591 |
UniProt ID | O94972 |
Synonyms | MUL; POB1; TEF3 |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | TRIM37 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 4591). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_001005207, NM_015294, NM_001320987, NM_001320988, NM_001320989, NM_001320990, NM_001353082, NM_001353083, NM_001353084, NM_001353085, NM_001353086, NR_148346, NR_148347, NM_001005207.1, NM_001005207.2, NM_001005207.3, NM_015294.1, NM_015294.2, NM_015294.3, NM_015294.4, BC036012, BC036012.1, NM_001005207.5, NM_015294.6 |
Summary | This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. Mutations in this gene are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. TRIM37 localizes in peroxisomal membranes, and has been implicated in human peroxisomal biogenesis disorders. [provided by RefSeq, Jul 2020] |
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). |
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