Plasmid pCMV·SPORT-βgal
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Invitrogen™

Plasmid pCMV·SPORT-βgal

Plasmid pCMV·SPORT-bgal is used as a positive control formonitoring expression in eukaryotic cells. The plasmid contains thereporter gene b-galactosidase (b-gal)Read more
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Catalog NumberQuantity
1058601425 μg
Catalog number 10586014
Price (USD)
820.00
Each
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Quantity:
25 μg
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Price (USD)
820.00
Each
Add to cart
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Plasmid pCMV·SPORT-bgal is used as a positive control for
monitoring expression in eukaryotic cells. The plasmid contains the
reporter gene b-galactosidase (b-gal) from E. coli cloned as a Not I
fragment into plasmid pCMV·SPORT1. The plasmid also contains
a CMV promoter upstream of the b-gal gene, followed by the SV40
t-intron and polyadenylation signal. The b-lactamase gene allows
selection for ampicillin resistance in E. coli.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Constitutive or Inducible SystemConstitutive
Delivery TypeTransfection
For Use With (Application)Reporter Assays, Constitutive Expression
Product TypePlasmid
Quantity25 μg
Reporter GeneBeta-Gal (lacZ)
Selection Agent (Eukaryotic)None
Shipping ConditionApproved for shipment on Wet or Dry Ice
VectorpCMV
PromoterCMV
Protein TagUntagged
Unit SizeEach
Contents & Storage
Store at +4°C. Store at -20°C long term.
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Frequently asked questions (FAQs)

How do I resuspend IPTG and X-Gal?

IPTG can be reconstituted in water. Make a stock of 100 mM in water and store working aliquots at -20°C. X-gal can be reconstituted in DMSO, or in a 50:50 mix of DMSO and water. To do the latter, you must dissolve in DMSO first, and then add water to bring up to final volume. It is not necessary to filter sterilize these solutions.

The X-gal solution should be protected from light. To make plates, add 50 ug/ml X-gal and 1 mM (0.24 mg/mL) IPTG to LB/agar that has been cooled down to 50°C. To spread on top of plates, use 50 µl 2% stock of X-gal and 30 µl 100 mM stock of IPTG. 

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

I sequenced one of your vectors after PCR amplification and observed a difference from what is provided online (or in the manual). Should I be concerned?

Our vectors have not been completely sequenced. Your sequence data may differ when compared to what is provided. Known mutations that do not affect the function of the vector are annotated in public databases.

Are your vectors routinely sequenced?

No, our vectors are not routinely sequenced. Quality control and release criteria utilize other methods.

How was the reference sequence for your vectors created?

Sequences provided for our vectors have been compiled from information in sequence databases, published sequences, and other sources.

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Lot #Certificate TypeDateCatalog Number(s)
3160300Certificate of AnalysisJul 14, 202510586014
3072410Certificate of AnalysisJan 10, 202510586014
2970278Certificate of AnalysisMay 28, 202410586014
2764104Certificate of AnalysisMay 13, 202410586014
2623440Certificate of AnalysisJul 11, 202310586014
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Safety Data Sheets

Vector Information

Vector Name
Vector Map
Polylinker
Sequence
Restriction
pPIC6alpha

Product Information

Citations & References (1)

Citations & References
Abstract
TNF-RII and c-IAP1 mediate ubiquitination and degradation of TRAF2.
Authors: Li Xiaoming; Yang Yili; Ashwell Jonathan D;
Journal:Nature
PubMed ID:11907583
Tumour necrosis factor-alpha (TNF-alpha) is a proinflammatory mediator that exerts its biological functions by binding two TNF receptors (TNF-RI and TNF-RII), which initiate biological responses by interacting with adaptor and signalling proteins. Among the signalling components that associate with TNF receptors are members of the TNF-R-associated factor (TRAF) family. TRAF2 ... More
1 total citations

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