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You are here:Home » Cloning » Cloning-Primers » Oct4 (POU Domain, Class 5, Transcription Factor 1 Oct3/4, POU5F1, HGNC:9221, MGC22487, Octamer-binding Transcription Factor 3, Oct3, OTF3, OTF4, POU-type Homeodomain-containing DNA-binding Protein), Mouse, Rat, Primer Pair

Oct4 (POU Domain, Class 5, Transcription Factor 1 Oct3/4, POU5F1, HGNC:9221, MGC22487,
Octamer-binding Transcription Factor 3, Oct3, OTF3, OTF4, POU-type Homeodomain-containing
DNA-binding Protein), Mouse, Rat, Primer Pair

Pricing

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Specifications

Mouse/rat Oct-3/4 (POU domain, class 5, transcription factor 1) specific PCR primers for RT-PCR (reverse transcription followed by polymerase chain reaction) analysis of mRNA expression.
Catalog #O5403-01G
ComponentsPrimer Pair: Lyophilized. Each vial contains 375 pmoles of each primer. Adjust to a final concentration of 7.5 pmoles/ul by resuspending Primer Pair in either 50ul autoclaved deionized water or 0.1X TE buffer (1mM Tris HCl, pH8.0 @ 25°C; 0.1mM EDTA, pH 8.0 @ 25°C).
Positive Control 59 Lyophilized. Each vial contains 150 ng synthetic double-stranded DNA. Resuspend in 30ul autoclaved deionized water or TE buffer. To prevent contaminating samples and reagents, it is strongly recommended that the Positive Control is resuspended in a separate location from where PCR reactions are set up. Use a different pipette than one used for PCR set up. The Positive Control is not intended for quantitative purposes.
GenBank Accession NumberNM_013633 (mouse) and NM_001009178 (rat)
Product SizescDNA: 536 base pairs (bp) (mouse), 537 bp (rat)
Genomic DNA: 2678 bp product predicted but not observed for mouse. 1191 bp product predicted and observed for rat. Products observed from pseudogenes at 536 bp for both mouse and rat. Treatment of RNA with RNase-free DNase is recommended to remove contaminating genomic DNA.
Positive Control 59: 290 bp
Alternate splice variants: None reported.
Suggested Reaction ConditionsFor each 50ul Polymerase Chain Reaction mixture, 2ul of the primer pair stock solution should be used. Sufficient reagent is supplied for 25 separate amplification reactions of the gene fragment.
Thermocycling ConditionsA typical 50ul PCR would involve a 4 minute denaturation step at 94ºC, followed by 30-35 cycles of 45 seconds at 94ºC, 45 seconds at 55ºC and 45 seconds at 72ºC, with a final 10 minute extension step at 72ºC.
Storage and StabilityThe Primer Pair resuspended in water or TE buffer is stable for up to one year at -20°C in a non-frost free freezer. Aliquot in single use portions. Do not use past the expiration date above. Avoid repeated freeze-thaw cycles.
Important NoteThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.


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