United States
Germany
Japan
United Kingdom
China
BLM (NM_000057) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC216075L3V
- LentiORF®
-
Lenti ORF particles, BLM (Myc-DDK tagged) - Human Bloom syndrome, RecQ helicase-like (BLM), 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 11,210.00
货期*
详询
规格
Product images
经常一起买 (3)
Specifications
| Product Data | |
| Product Name | BLM (NM_000057) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BS; MGRISCE1; RECQ2; RECQL2; RECQL3 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_000057 |
| ORF Size | 4251 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC216075).
|
| 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_000057.1 |
| RefSeq Size | 4437 bp |
| RefSeq ORF | 4254 bp |
| Locus ID | 641 |
| Protein Families | Druggable Genome, Stem cell - Pluripotency |
| Protein Pathways | Homologous recombination |
| MW | 158.8 kDa |
| Gene Summary | The Bloom syndrome is an autosomal recessive disorder characterized by growth deficiency, microcephaly and immunodeficiency among others. It is caused by homozygous or compound heterozygous mutation in the gene encoding DNA helicase RecQ protein on chromosome 15q26. This Bloom-associated helicase unwinds a variety of DNA substrates including Holliday junction, and is involved in several pathways contributing to the maintenance of genome stability. Identification of pathogenic Bloom variants is required for heterozygote testing in at-risk families. [provided by RefSeq, May 2020] |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
You may also need
Customer
Reviews
Loading...
