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HomeAdvanced Gene EditingSnapFast™ Cloning & Expression Vectors Selection Charts

SnapFast™ Cloning & Expression Vectors Selection Charts

With over 1600 vectors to choose from, your options may seem endless. For help choosing the right vector for your research needs, consult the tables below.

Bacterial vector options with FLAG and 3xFLAG tags

Mammalian vector options with FLAG and 3xFLAG tags

Vector options for secretory tags for use in bacterial cells

Vector options for secretory tags for use in yeast cells

Vector options for secretory tags for use in mammalian cells

Vector options for single functional tags for use in yeast cells

Yeast Plasmids Encoding Single Functional Tags

N Terminal Tag Plasmids are in Blue
C Terminal Tag Plasmids are in Red

Vector options for dual functional tags for use in yeast cells

Yeast Plasmids Encoding Dual Functional Tags

N Terminal Tag Plasmids are in Blue
C Terminal Tag Plasmids are in Red

Vector options for fluorescent reporters

Fluorescence Reporter Gene Plasmids

NOTES:

(a)PromMCS plasmids have no promoter driving the reporter gene, but they have several unique restriction sites that can be used to insert the promoter of your choice.

(b)MinProm plasmids contain the minimal HSV TK promoter driving the reporter gene, with an upstream MCS that can be used to introduce specificity-defining sequences (such as transcription factor binding sites) of your choice

(c)CMVe plasmids contain the CMV enhancer upstream of the MCS, for your to insert your promoter of choice. The CMV enhancer should augment its activity.

Vector options for fusion reporters

Mammalian Reporter Fusion Protein Plasmids

N Terminal Tag Plasmids are in Blue
C Terminal Tag Plasmids are in Red

Vector options for the Luciferase reporter

Luciferase Reporter Gene Plasmids

NOTES:

(a)PromMCS plasmids have no promoter driving the reporter gene, but they have several unique restriction sites that can be used to insert the promoter of your choice.

(b)MinProm plasmids contain the minimal HSV TK promoter driving the reporter gene, with an upstream MCS that can be used to introduce specificity-defining sequences (such as transcription factor binding sites) of your choice

(c)CMVe plasmids contain the CMV enhancer upstream of the MCS, for your to insert your promoter of choice. The CMV enhancer should augment its activity.

Vector options for Colorimetric reporters

Colorimetric Reporter Gene Plasmids

NOTES:

(a)PromMCS plasmids have no promoter driving the reporter gene, but they have several unique restriction sites that can be used to insert the promoter of your choice.

(b)MinProm plasmids contain the minimal HSV TK promoter driving the reporter gene, with an upstream MCS that can be used to introduce specificity-defining sequences (such as transcription factor binding sites) of your choice

(c)CMVe plasmids contain the CMV enhancer upstream of the MCS, for your to insert your promoter of choice. The CMV enhancer should augment its activity.

Looking for more vector options to move your experiments forward faster? Consider a custom cloning vector designed and built by Oxford Genetics™. Find out more at Oxford Genetics - our partner for cloning and expression vectors for molecular biology and synthetic biology applications.

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