Nicotinic Acetylcholine Receptor alpha 7 (CHRNA7) Human shRNA Plasmid Kit (Locus ID 1139)

SKU
TG313917
CHRNA7 - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector, 5µg of each construct provided
  $883.00
In Stock*
Specifications
Specifications
Product Data
Locus ID 1139
Synonyms CHRNA7-2; NACHRA7
Vector pGFP-V-RS
E. coli Selection Kanamycin
Format Retroviral plasmids
Components CHRNA7 - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 1139). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free.
RefSeq NM_000746, NM_001190455, NR_046324, NM_000746.1, NM_000746.2, NM_000746.3, NM_000746.4, NM_000746.5, NM_001190455.1, NM_001190455.2, BC037571, BC037571.1, BM451308, NM_001190455.3, NM_000746.6
UniProt ID P36544
Summary The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The nAChRs are thought to be hetero-pentamers composed of homologous subunits. The proposed structure for each subunit is a conserved N-terminal extracellular domain followed by three conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region. The protein encoded by this gene forms a homo-oligomeric channel, displays marked permeability to calcium ions and is a major component of brain nicotinic receptors that are blocked by, and highly sensitive to, alpha-bungarotoxin. Once this receptor binds acetylcholine, it undergoes an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. This gene is located in a region identified as a major susceptibility locus for juvenile myoclonic epilepsy and a chromosomal location involved in the genetic transmission of schizophrenia. An evolutionarily recent partial duplication event in this region results in a hybrid containing sequence from this gene and a novel FAM7A gene. Alternative splicing results in multiple transcript variants. provided by RefSeq, Feb 2012
shRNA Design These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact techsupport@origene.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service.
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