Gliomedin (GLDN) (NM_181789) Human Tagged ORF Clone Lentiviral Particle
SKU
RC214259L4V
Lenti ORF particles, GLDN (mGFP-tagged) - Human gliomedin (GLDN), 200ul, >10^7 TU/mL
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
---|---|
Tag | mGFP |
Target Symbol | Gliomedin |
Synonyms | CLOM; COLM; CRG-L2; CRGL2; LCCS11; UNC-112; UNC-122 |
Vector | pLenti-C-mGFP-P2A-Puro |
Mammalian Cell Selection | Puromycin |
Sequence Data |
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC214259).
|
ACCN | NM_181789 |
ORF Size | 1653 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. |
Shipping | Dry Ice |
Reference Data | |
RefSeq | NM_181789.2 |
RefSeq Size | 5084 bp |
RefSeq ORF | 1656 bp |
Locus ID | 342035 |
UniProt ID | Q6ZMI3 |
Cytogenetics | 15q21.2 |
Protein Families | Transmembrane |
MW | 58.8 kDa |
Summary | This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017] |
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