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Aff1 (NM_001080798) Mouse Tagged ORF Clone Lentiviral Particle
CAT＃: MR219379L3V
- LentiORF®
-
Lenti ORF particles, Aff1 (Myc-DDK-tagged) - Mouse AF4/FMR2 family, member 1 (Aff1), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 17,765.00
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Specifications
| Product Data | |
| Product Name | Aff1 (NM_001080798) Mouse Tagged ORF Clone Lentiviral Particle |
| Synonyms | 9630032B01Rik; Af; Af4; AW319193; Mllt; Mllt2h; R; Rob |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_001080798 |
| ORF Size | 3678 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(MR219379).
|
| 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_001080798.1, NP_001074267.1 |
| RefSeq Size | 8312 bp |
| RefSeq ORF | 3681 bp |
| Locus ID | 17355 |
| Gene Summary | This gene encodes a member of the AF4/ lymphoid nuclear protein related to the Fragile X E syndrome (FRAXE) family of proteins, which have been implicated in human childhood lymphoblastic leukemia, fragile chromosome X intellectual disability, and ataxia. It is the prevalent mixed-lineage leukemia fusion gene associated with spontaneous acute lymphoblastic leukemia. Members of this family have three conserved domains: an N-terminal homology domain, an AF4/ lymphoid nuclear protein domain, and a C-terminal homology domain. Knockout of the mouse gene by homologous recombination severely affects early events in lymphopoiesis, including precursor proliferation or recruitment, but is dispensable for terminal differentiation. In addition, an autosomal dominant missense mutation results in several phenotypes including ataxia and adult-onset Purkinje cell loss in the cerebellum, indicating a role in Purkinje cell maintenance and function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017] |
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