Crbn (NM_175357) Mouse Tagged ORF Clone

CAT#: MR225531L3

  • LentiORF®

Lenti ORF clone of Crbn (Myc-DDK-tagged) - Mouse cereblon (Crbn), transcript variant 2


  "NM_175357" in other vectors (4)


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Reconstitution Protocol

USD 670.00

In Stock*

Size
    • 10 ug

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Specifications

Product Data
Type Mouse Tagged ORF Clone
Tag Myc-DDK
Symbol Crbn
Synonyms 2610203G15Rik; 2900045O07Rik; AF229032; AW108261; piL
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(MR225531).
Restriction Sites SgfI-MluI      Cloning Scheme for this gene     
ACCN NM_175357
ORF Size 1335 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_175357.2, NP_780566.1
RefSeq Size 4054
RefSeq ORF 1338
Locus ID 58799
Gene Summary This gene encodes a protein with a Lon protease domain, a "regulators of G protein-signaling" (RGS)-like domain and a leucine zipper. It has been proposed to regulate the assembly and surface expression of large-conductance calcium-activated potassium channels in brain and to bind thalidomide. In humans mutation in this gene causes autosomal recessive nonsyndromic cognitive disability. In mouse deficiency of this gene serves as a model to study the molecular mechanisms governing learning and memory as they relate to intellectual disability. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jan 2013]

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