MSX1 (NM_002448) Human Tagged ORF Clone

CAT#: RC205682L4

  • LentiORF®

Lenti ORF clone of Human msh homeobox 1 (MSX1), mGFP tagged

  View "NM_002448" in other vectors (11)

Save 30% on Lenti Packaging Kit

USD 760.00

3 Weeks

    • 10 ug

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Product Data
Product Name MSX1 (NM_002448) Human Tagged ORF Clone
Symbol MSX1
Synonyms ECTD3; HOX7; HYD1; STHAG1
Vector pLenti-C-mGFP-P2A-Puro
Sequence Data
The ORF insert of this clone is exactly the same as(RC205682).
Restriction Sites SgfI-MluI      Cloning Scheme for this gene     
Tag mGFP
ACCN NM_002448
ORF Size 909 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.
Product Components The ORF clone is ion-exchange column purified, transfection-ready dried plasmid DNA, and shipped with 2 vector sequencing primers.
Reference Data
RefSeq NM_002448.3, NP_002439
RefSeq Size 1940
RefSeq ORF 912
Locus ID 4487
Cytogenetics 4p16.2
Domains homeobox
Protein Families Transcription Factors, Druggable Genome
MW 31.3 kDa
Gene Summary This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq, Jul 2008].

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*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.
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