TRIM37 (NM_015294) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC224302L1V

  • LentiORF®

Lenti ORF particles, TRIM37 (Myc-DDK tagged) - Human tripartite motif containing 37 (TRIM37), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



Need custom lentivirus service?
Get a free quote

CNY 17,005.00


货期*
详询

规格
    • 200 ul

Cited in 1 publication.

Product images

经常一起买 (3)
Lenti ORF control particles of pLenti-C-Myc-DDK, >10^7 TU/mL, 0.5 mL
    • 500 ul

CNY 2,950.00


One-Wash Lentivirus Titer Kit, HIV-1 p24 ELISA
    • 96 reactions

CNY 5,230.00


TRIM37 Antibody - middle region
    • 50 ug

CNY 4,628.00

Specifications

Product Data
Product Name TRIM37 (NM_015294) Human Tagged ORF Clone Lentiviral Particle
Synonyms MUL; POB1; TEF3
Vector pLenti-C-Myc-DDK
ACCN NM_015294
ORF Size 2892 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC224302).
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_015294.2
RefSeq Size 4488 bp
RefSeq ORF 2895 bp
Locus ID 4591
Domains zf-B_box, MATH, BBC
Protein Families Druggable Genome
Protein Pathways Ubiquitin mediated proteolysis
MW 107.7 kDa
Gene Summary This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. Mutations in this gene are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. TRIM37 localizes in peroxisomal membranes, and has been implicated in human peroxisomal biogenesis disorders. [provided by RefSeq, Jul 2020]
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Citations (1)

Customer Reviews 
Loading...