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RC200862L2V

robld3 (LAMTOR2) (NM_014017) Human Tagged ORF Clone Lentiviral Particle

Origene Technologies, Inc.

DESCRIPTION

Lenti ORF particles, LAMTOR2 (mGFP-tagged) - Human late endosomal/lysosomal adaptor, MAPK and MTOR activator 2 (LAMTOR2), transcript variant 1, 200ul, >10^7 TU/mL

DETAILS

  • Mw: 13.5 kDa
  • Tag: mGFP
  • Accn: NM_014017
  • Type: Human Tagged ORF Clone Lentiviral Particle
  • Refseq: NM_014017.1
  • Status: 7 Weeks*
  • Symbol: LAMTOR2
  • Vector: pLenti-C-mGFP
  • Category: cDNA Clones
  • Locus Id: 28956
  • Orf Size: 375 bp
  • Synonyms: ENDAP; HSPC003; MAPBPIP; MAPKSP1AP; p14; Ragulator2; ROBLD3
  • Refseq Orf: 378 bp
  • Uniprot Id: Q9Y2Q5
  • Refseq Size: 699 bp
  • Availability: 7 Weeks
  • Cytogenetics: 1q22
  • Gene Summary: The product of this gene is highly conserved with a mouse protein associated with the cytoplasmic face of late endosomes and lysosomes. The mouse protein interacts with MAPK scaffold protein 1, a component of the mitogen-activated protein kinase pathway. In humans, a mutation in this gene has been associated with a primary immunodeficiency syndrome, and suggests a role for this protein in endosomal biogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]
  • Sequence Data: ORF Nucleotide Sequence ( show hide ) The ORF insert of this clone is exactly the same as(RC200862).
  • Oti Annotation: This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
  • 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
  • Mammalian Cell Selection: None