Crmp1 (NM_007765) Mouse Tagged ORF Clone

CAT#: MR209012L3

  • LentiORF®

Lenti ORF clone of Crmp1 (Myc-DDK-tagged) - Mouse collapsin response mediator protein 1 (Crmp1), transcript variant 2


  "NM_007765" in other vectors (4)


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Reconstitution Protocol

USD 730.00

3 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Mouse Tagged ORF Clone
Tag Myc-DDK
Symbol Crmp1
Synonyms CRMP-1; Dpysl1; DRP-1; ULIP-3; Ulip3
Vector pLenti-C-Myc-DDK-P2A-Puro
E. coli Selection Chloramphenicol (34 ug/mL)
Mammalian Cell Selection Puromycin
Sequence Data
The ORF insert of this clone is exactly the same as(MR209012).
Restriction Sites SgfI-MluI      Cloning Scheme for this gene     
ACCN NM_007765
ORF Size 1716 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.
Reference Data
RefSeq NM_007765.3, NP_031791.3
RefSeq Size 2968
RefSeq ORF 1719
Locus ID 12933
Gene Summary This gene encodes a protein that is part of the collapsin response mediator protein family. The family is comprised of five, homologous cytosolic phosphoproteins that are expressed in developing and adult nervous tissue and mediate signaling to transduce responses to extracellular cues. This protein is a Semaphorin 3A signaling molecule that regulates collapse of the growth cone. The growth cone mediates axonal pathfinding in neurons. This protein is reported to represent a new class of microtubule-associated proteins. In humans this protein is reported to inhibit cancer cell invasion. In mouse deficiency of this gene may be associated with impaired spatial memory performance. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jan 2013]

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