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Hexa (NM_010421) Mouse Tagged ORF Clone Lentiviral Particle
CAT＃: MR208464L3V
- LentiORF®
-
Lenti ORF particles, Hexa (Myc-DDK-tagged) - Mouse hexosaminidase A (Hexa), 200ul, >10^7 TU/mL
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CNY 9,785.00
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规格
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Specifications
| Product Data | |
| Product Name | Hexa (NM_010421) Mouse Tagged ORF Clone Lentiviral Particle |
| Synonyms | Hex-1 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_010421 |
| ORF Size | 1587 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(MR208464).
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| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_010421.3 |
| RefSeq Size | 1865 bp |
| RefSeq ORF | 1587 bp |
| Locus ID | 15211 |
| Gene Summary | This gene encodes a member of the glycosyl hydrolase 20 family of proteins. The encoded preproprotein is proteolytically processed to generate the alpha subunit of the lysosomal enzyme beta-hexosaminidase. This enzyme, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mice lacking the encoded protein exhibit accumulation of gangliosides in the brain and membranous cytoplasmic bodies in neurons. Certain mutations in the human ortholog of this gene cause Tay-Sachs disease. [provided by RefSeq, Aug 2016] |
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