Uromucoid (UMOD) (NM_001008389) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC224496L3V
- LentiORF®
Lenti ORF particles, UMOD (Myc-DDK-tagged)-Human uromodulin (UMOD), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 11,115.00
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Specifications
Product Data | |
Product Name | Uromucoid (UMOD) (NM_001008389) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | ADMCKD2; ADTKD1; FJHN; HNFJ; HNFJ1; MCKD2; THGP; THP |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001008389 |
ORF Size | 1920 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC224496).
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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_001008389.1 |
RefSeq Size | 2264 bp |
RefSeq ORF | 1923 bp |
Locus ID | 7369 |
MW | 69.76 kDa |
Gene Summary | The protein encoded by this gene is the most abundant protein in mammalian urine under physiological conditions. Its excretion in urine follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinosital-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. This protein may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of this protein in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the renal disorders medullary cystic kidney disease-2 (MCKD2), glomerulocystic kidney disease with hyperuricemia and isosthenuria (GCKDHI), and familial juvenile hyperuricemic nephropathy (FJHN). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
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