APXL (SHROOM2) (NM_001649) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC222295L1V

  • LentiORF®

Lenti ORF particles, SHROOM2 (Myc-DDK-tagged)-Human shroom family member 2 (SHROOM2), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK DDK w/ Puro mGFP mGFP w/ Puro


Biosafety Sheet

USD 1,932.00

2 Weeks*

Size
    • 200 ul

Product Images

Frequently bought together (3)
Lenti ORF control particles of pLenti-C-Myc-DDK, >10^7 TU/mL, 0.5 mL
    • 500 ul

USD 365.00


One-Wash Lentivirus Titer Kit, HIV-1 p24 ELISA
    • 96 reactions

USD 671.00


Rabbit Polyclonal Anti-SHROOM2 Antibody
    • 100 ul

USD 380.00

Other products for "APXL"

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol APXL
Synonyms APXL; HSAPXL
Mammalian Cell Selection None
Vector pLenti-C-Myc-DDK
ACCN NM_001649
ORF Size 4848 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC222295).
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_001649.2
RefSeq Size 7445 bp
RefSeq ORF 4851 bp
Locus ID 357
UniProt ID Q13796
Cytogenetics Xp22.2
Protein Families Druggable Genome
MW 176.2 kDa
Gene Summary This gene represents the human homolog of Xenopus laevis apical protein (APX) gene, which is implicated in amiloride-sensitive sodium channel activity. It is expressed in endothelial cells and facilitates the formation of a contractile network within endothelial cells. Depletion of this gene results in an increase in endothelial sprouting, migration, and angiogenesis. This gene is highly expressed in the retina, and is a strong candidate for ocular albinism type 1 syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016]

{0} Product Review(s)

0 Product Review(s) Submit review

Be the first one to submit a review

Product Citations

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.