Difference between revisions of "Part:BBa K1763434"

Latest revision as of 21:11, 18 September 2015

MaSp1-9(1C3)

This is a 9-mer construct of MaSp1 constructed using Iterative Capped Assembly (ICA) protocols as outlined on the 2015 UCLA iGEM page [http://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/Protocols here]. This part is a coding sequence, with no regulatory elements present. This construct includes an N-terminal 8-his tag which can be used purify this protein using nickel based affinity purification techniques.

Biology

Native spider silk genes consist of many repeats of the MaSp genes, up to 100 repeats. The extensive repetition confers the properties of strength and elasticity that are commonly associated with spider silk threads. In order to examine the role of protein length and composition on the final properties of spider silk, we created this construct using Iterative Capped Assembly.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
INCOMPATIBLE WITH RFC[21]
Illegal BamHI site found at 958
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
COMPATIBLE WITH RFC[1000]

Usage

In order to express this construct as a protein, it is necessary to subclone it after a promoter and RBS. The 2015 UCLA iGEM team has made a composite part, BBa_K1763435, has placed this part under control of the T7-RBS regulatory elements.

This construct was successfully amplified using the [http://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/ICA_Oligo_Sequences post-elution primers] after ICA. The results of the amplification are shown below.

Fig. 1 PCR amplification of MaSp1-9 using post-elution primers. The expected product size is 1018 bp.

@@ Line 1: / Line 1: @@
 __NOTOC__
 <partinfo>BBa_K1763434 short</partinfo>
-MaSp1 9 mer in pSB1C3, no regulatory elements present.
+This is a 9-mer construct of MaSp1 constructed using Iterative Capped Assembly (ICA) protocols as outlined on the 2015 UCLA iGEM page [http://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/Protocols here]. This part is a coding sequence, with no regulatory elements present. This construct includes an N-terminal 8-his tag which can be used purify this protein using nickel based affinity purification techniques.
-<!-- Add more about the biology of this part here
+<!-- Add more about the biology of this part here -->
-===Usage and Biology===
+===Biology===
+Native spider silk genes consist of many repeats of the MaSp genes, up to 100 repeats. The extensive repetition confers the properties of strength and elasticity that are commonly associated with spider silk threads. In order to examine the role of protein length and composition on the final properties of spider silk, we created this construct using Iterative Capped Assembly.
 <!-- -->
@@ Line 12: / Line 12: @@
 <partinfo>BBa_K1763434 SequenceAndFeatures</partinfo>
+===Usage===
+In order to express this construct as a protein, it is necessary to subclone it after a promoter and RBS. The 2015 UCLA iGEM team has made a composite part, [https://parts.igem.org/Part:BBa_K1763435 BBa_K1763435], has placed this part under control of the T7-RBS regulatory elements.
+This construct was successfully amplified using the [http://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics/ICA_Oligo_Sequences post-elution primers] after ICA. The results of the amplification are shown below.
+[[File:7 30 2015 UCLA ICA 9mer.jpg|none|thumb|500px|'''Fig. 1''' PCR amplification of MaSp1-9 using post-elution primers. The expected product size is 1018 bp.]]
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