Difference between revisions of "Part:BBa K5198100"
(One intermediate revision by the same user not shown) | |||
Line 3: | Line 3: | ||
<partinfo>BBa_K5198100 short</partinfo> | <partinfo>BBa_K5198100 short</partinfo> | ||
<html> | <html> | ||
+ | <br> | ||
SEAP acts as a continuous quantitative reporter for gene expression by repeatedly assessing the activity of certain promoter/enhancer elements in many cell samples. SEAP is contained in exosomes and is normally secreted into the extracellular space. This reporter’s activity can be assayed quicker, more easily, and more cheaply than other reporter enzymes’ activities. SEAP activity can be detected with conventional chemiluminescent assays. HA-SEAP is a SEAP (<a href="http://parts.igem.org/Part:BBa_K1470004">BBa_K1470004</a>) with an HA tag (<a href="http://parts.igem.org/Part:BBa_K1150016">BBa_K1150016</a>). The part can be used as a negative control in secretion studies as HA tag does not signal extracellular export of the protein (<b>Figure 1</b>). | SEAP acts as a continuous quantitative reporter for gene expression by repeatedly assessing the activity of certain promoter/enhancer elements in many cell samples. SEAP is contained in exosomes and is normally secreted into the extracellular space. This reporter’s activity can be assayed quicker, more easily, and more cheaply than other reporter enzymes’ activities. SEAP activity can be detected with conventional chemiluminescent assays. HA-SEAP is a SEAP (<a href="http://parts.igem.org/Part:BBa_K1470004">BBa_K1470004</a>) with an HA tag (<a href="http://parts.igem.org/Part:BBa_K1150016">BBa_K1150016</a>). The part can be used as a negative control in secretion studies as HA tag does not signal extracellular export of the protein (<b>Figure 1</b>). | ||
<div style="text-align: center;"> | <div style="text-align: center;"> | ||
− | <img src="https://static.igem.wiki/teams/5198/results/figure-4v3.webp" alt="Description of the image"> | + | <img src="https://static.igem.wiki/teams/5198/results/figure-4v3.webp" alt="Description of the image" width="400"> |
</div> | </div> | ||
<p>Figure 1. Chemiluminescent readings of SEAP with different signal peptide fusions in HEK293T cell supernatant. The negative control (NC) is SEAP fused with an HA tag, which does not signal extracellular secretion. Error bars represent the standard deviation (SD) of 4 biological replicates. The data was normalized by subtracting background fluorescence. </p> | <p>Figure 1. Chemiluminescent readings of SEAP with different signal peptide fusions in HEK293T cell supernatant. The negative control (NC) is SEAP fused with an HA tag, which does not signal extracellular secretion. Error bars represent the standard deviation (SD) of 4 biological replicates. The data was normalized by subtracting background fluorescence. </p> |
Latest revision as of 10:07, 2 October 2024
HA-SEAP
SEAP acts as a continuous quantitative reporter for gene expression by repeatedly assessing the activity of certain promoter/enhancer elements in many cell samples. SEAP is contained in exosomes and is normally secreted into the extracellular space. This reporter’s activity can be assayed quicker, more easily, and more cheaply than other reporter enzymes’ activities. SEAP activity can be detected with conventional chemiluminescent assays. HA-SEAP is a SEAP (BBa_K1470004) with an HA tag (BBa_K1150016). The part can be used as a negative control in secretion studies as HA tag does not signal extracellular export of the protein (Figure 1).
Figure 1. Chemiluminescent readings of SEAP with different signal peptide fusions in HEK293T cell supernatant. The negative control (NC) is SEAP fused with an HA tag, which does not signal extracellular secretion. Error bars represent the standard deviation (SD) of 4 biological replicates. The data was normalized by subtracting background fluorescence.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 236
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 547
Illegal NgoMIV site found at 1516 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 877
Illegal BsaI.rc site found at 1366