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Home cDNA Clone TrueORF All F2 ORF Clones

F2 (NM_000506) Human cDNA ORF Clone

Specifications Citations Clone of Other Species Product Documents
Cat. No. Description Price Availability  
RG208589 GFP-tagged ORF clone of Homo sapiens coagulation factor II (thrombin) (F2) as transfection-ready DNA, 10µg
$590
In Stock

$50 off anti-DDK and other anti-tag antibodies till June 30th, 2013

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Also for F2 (NM_000506)
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TrueORF Data for RG208589
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Vector: pCMV6-AC-GFP   Change vector? Tag: C-terminal TurboGFP
Sequence Data: ORF Nucleotide Sequence
Protein Sequence
ORF Size: 1869 bp
Restriction Sites: SgfI-MluI     Cloning Scheme for this gene     Plasmid Map Plasmid Map
OTI Annotation: This clone was engineered to express the complete ORF with an expression tag.
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
Product Components: The ORF clone is ion-exchange column purified, transfection-ready dried plasmid DNA, and shipped with 2 vector sequencing primers.
Protein Families: Secreted ProteinProteaseDruggable Genome
Protein Pathways: Neuroactive ligand-receptor interactionComplement and coagulation cascadesRegulation of actin cytoskeleton
* The lysates used for this WB picture contain the overexpressed empty vector or the Myc-DDK tagged ORF clone.

Reference Data
RefSeq: NM_000506.2, NP_000497
RefSeq Size: 1997 RefSeq ORF: 1869
Synonyms : PT; RPRGL2; THPH1
LocusID: 2147 Cytogenetic: 11p11 Domains: KR, gla, Tryp_SPc
Summary: Coagulation factor II is proteolytically cleaved to form thrombin in the first step of the coagulation cascade which ultimately results in the stemming of blood loss. F2 also plays a role in maintaining vascular integrity during development and postnatal life. Mutations in F2 leads to various forms of thrombosis and dysprothrombinemia. [provided by RefSeq, Jul 2008].

 

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