SLC26A4 (NM_000441) Human Tagged ORF Clone Lentiviral Particle
SKU
RC222532L2V
Lenti ORF particles, SLC26A4 (mGFP-tagged) - Human solute carrier family 26, member 4 (SLC26A4), 200ul, >10^7 TU/mL
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
---|---|
Tag | mGFP |
Target Symbol | SLC26A4 |
Synonyms | DFNB4; EVA; PDS; TDH2B |
Vector | pLenti-C-mGFP |
Mammalian Cell Selection | None |
Sequence Data |
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC222532).
|
ACCN | NM_000441 |
ORF Size | 2340 bp |
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. |
Shipping | Dry Ice |
Reference Data | |
RefSeq | NM_000441.1 |
RefSeq Size | 4930 bp |
RefSeq ORF | 2343 bp |
Locus ID | 5172 |
UniProt ID | O43511 |
Cytogenetics | 7q22.3 |
Domains | STAS, Sulfate_transp |
Protein Families | Druggable Genome, Transmembrane |
MW | 85.5 kDa |
Summary | Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008] |
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