alpha 1 Catenin (CTNNA1) (NM_001903) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC201766L1V
- LentiORF®
Lenti ORF particles, CTNNA1 (Myc-DDK tagged) - Human catenin (cadherin-associated protein), alpha 1, 102kDa (CTNNA1), 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | CTNNA1 |
Synonyms | CAP102; MDPT2 |
Vector | pLenti-C-Myc-DDK |
ACCN | NM_001903 |
ORF Size | 2718 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC201766).
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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_001903.2, NP_001894.2 |
RefSeq Size | 3791 bp |
RefSeq ORF | 2721 bp |
Locus ID | 1495 |
Cytogenetics | 5q31.2 |
Domains | Vinculin |
Protein Families | Druggable Genome |
Protein Pathways | Adherens junction, Arrhythmogenic right ventricular cardiomyopathy (ARVC), Endometrial cancer, Leukocyte transendothelial migration, Pathways in cancer, Tight junction |
MW | 100.1 kDa |
Gene Summary | 'This gene encodes a member of the catenin family of proteins that play an important role in cell adhesion process by connecting cadherins located on the plasma membrane to the actin filaments inside the cell. The encoded mechanosensing protein contains three vinculin homology domains and undergoes conformational changes in response to cytoskeletal tension, resulting in the reconfiguration of cadherin-actin filament connections. Certain mutations in this gene cause butterfly-shaped pigment dystrophy. [provided by RefSeq, May 2016]' |
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