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NBPF3 (NM_032264) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC215220L1V
- LentiORF®
-
Lenti ORF particles, NBPF3 (Myc-DDK-tagged)-Human neuroblastoma breakpoint family, member 3 (NBPF3), 200ul, >10^7 TU/mL
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CNY 11,020.00
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规格
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Specifications
| Product Data | |
| Product Name | NBPF3 (NM_032264) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | AE2 |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_032264 |
| ORF Size | 1899 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC215220).
|
| 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_032264.3 |
| RefSeq Size | 3783 bp |
| RefSeq ORF | 1902 bp |
| Locus ID | 84224 |
| MW | 72.8 kDa |
| Gene Summary | This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. DUF1220 copy number variations in human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Feb 2013] |
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