ANK1 (NM_020476) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC220763L1V
- LentiORF®
Lenti ORF particles, ANK1 (Myc-DDK tagged) - Human ankyrin 1, erythrocytic (ANK1), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 21,660.00
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Specifications
Product Data | |
Product Name | ANK1 (NM_020476) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | ANK; SPH1; SPH2 |
Vector | pLenti-C-Myc-DDK |
ACCN | NM_020476 |
ORF Size | 5643 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC220763).
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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_020476.2 |
RefSeq Size | 8240 bp |
RefSeq ORF | 5646 bp |
Locus ID | 286 |
Protein Families | Transmembrane |
MW | 206.1 kDa |
Gene Summary | Ankyrins are a family of proteins that link the integral membrane proteins to the underlying spectrin-actin cytoskeleton and play key roles in activities such as cell motility, activation, proliferation, contact and the maintenance of specialized membrane domains. Multiple isoforms of ankyrin with different affinities for various target proteins are expressed in a tissue-specific, developmentally regulated manner. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats; a central region with a highly conserved spectrin binding domain; and a carboxy-terminal regulatory domain which is the least conserved and subject to variation. Ankyrin 1, the prototype of this family, was first discovered in the erythrocytes, but since has also been found in brain and muscles. Mutations in erythrocytic ankyrin 1 have been associated in approximately half of all patients with hereditary spherocytosis. Complex patterns of alternative splicing in the regulatory domain, giving rise to different isoforms of ankyrin 1 have been described. Truncated muscle-specific isoforms of ankyrin 1 resulting from usage of an alternate promoter have also been identified. [provided by RefSeq, Dec 2008] |
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