mu Crystallin (CRYM) (NM_001888) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC218123L2V

  • LentiORF®

Lenti ORF particles, CRYM (mGFP-tagged) - Human crystallin, mu (CRYM), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

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

AAV Particle: DDK


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USD 850.00

7 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol mu Crystallin
Synonyms DFNA40; THBP
Mammalian Cell Selection None
Vector pLenti-C-mGFP
ACCN NM_001888
ORF Size 942 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC218123).
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_001888.2
RefSeq Size 1559 bp
RefSeq ORF 945 bp
Locus ID 1428
UniProt ID Q14894
Cytogenetics 16p12.2
Domains ODC_Mu_crystall
MW 33.8 kDa
Gene Summary Crystallins are separated into two classes: taxon-specific and ubiquitous. The former class is also called phylogenetically-restricted crystallins. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. This gene encodes a taxon-specific crystallin protein that binds NADPH and has sequence similarity to bacterial ornithine cyclodeaminases. The encoded protein does not perform a structural role in lens tissue, and instead it binds thyroid hormone for possible regulatory or developmental roles. Mutations in this gene have been associated with autosomal dominant non-syndromic deafness. [provided by RefSeq, Sep 2014]

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