Tg(Slc1a6-EGFP)#aRthsn
Transgene Detail
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| Symbol: |
Tg(Slc1a6-EGFP)#aRthsn |
| Name: |
transgene insertion #a, David Rothstein |
| MGI ID: |
MGI:7564210 |
| Transgene: |
Tg(Slc1a6-EGFP)#aRthsn Location: unknown
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| Alliance: |
Tg(Slc1a6-EGFP)#aRthsn page
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| Strain of Origin: |
C57BL/6 x SJL
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| Transgene Type: |
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Transgenic (Reporter) |
| Mutation: |
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Insertion
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Tg(Slc1a6-EGFP)#aRthsn expression driven by
1 gene
Transgene expression driven by:
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Mutation details: The EAAT4 start codon, in exon 2, was mutated to TTG, and the EGFP cDNA (Clontech) was inserted downstream, after the end of the A-box, within the same exon. Lines 41 and 61 was generated with line 41 exhibiting higher expression levels. Line #a represents the unspecified line used at the Crick Institute.
(J:270969)
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| Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
| Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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| Original: |
J:270969 Gincel D, et al., Analysis of cerebellar Purkinje cells using EAAT4 glutamate transporter promoter reporter in mice generated via bacterial artificial chromosome-mediated transgenesis. Exp Neurol. 2007 Jan;203(1):205-12 |
| All: |
3 reference(s) |
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