Expression Database

GUDMAP:11557
Data Source
Gene
Tnfsf8 tumor necrosis factor (ligand) superfamily, member 8
Theiler Stage TS23
Images
Development time: 24hrs.
Whole-mount in situ hybridization is subject to technical limitations that may influence accuracy of the data (more info).
Submitters
Principal Investigator(s): Andrew P McMahon, Harvard University, Cambridge, MA, USA, amcmahon@med.usc.edu
Authors: Andrew P McMahon, M Todd Valerius
Submitted By: M Todd Valerius, Harvard University, Cambridge, MA, USA, tvalerius@mcb.harvard.edu
Archive ID: 173
Submission ID: AM_190309_22
Expression Mapping

Expression Strengths Key:
Present (unspecified strength)
Present (strong)
Present (moderate)
Present (weak)
Uncertain
Not Detected
   
Expression Patterns Key:
Homogeneous
Graded
Regional
Spotted
Ubiquitous
Restricted
Single cell
Contains note
View annotated components as a list Show annotation under groups information
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Probe
Gene:
Symbol: Tnfsf8
Name: tumor necrosis factor (ligand) superfamily, member 8 (MGI:88328)
Probe ID: maprobe:5589
Name of cDNA: 5830454L09
Additional Name of cDNA: MSR1671
Sequence ID:
AK030916.1
5' primer sequence: ATGGAGCCAGGGCTGCAACA
3' primer sequence: TAATACGACTCACTATAGGGAGAAGACGGATAGCACAT
5' primer location: 227
3' primer location: 926
Origin of Clone used to make the Probe:
Strain: C57BL/6
  Tissue: brain
Probe Type: RNA
Type: antisense
Labelled with: digoxigenin
Visualisation method: alkaline phosphatase + BM purple
Lab Probe ID: 758
Probe Notes: Probe template was amplified from RIKEN clone 5830454L09 using primers designed to the coding region. A T7 promoter sequence was added to the reverse primer for probe transcription. The primers used: Reverse primer sequence = TAATACGACTCACTATAGGGAGAAGACGGATAGCACAT : Forward primer sequence= ATGGAGCCAGGGCTGCAACA. MSR1671.
Specimen
Theiler Stage: TS23
Other Staging System: 15.5dpc
Tissue:
Strain: Swiss Webster
Genotype: Wild type
Sex: female
Specimen Preparation:
wholemount
Fixation Method: 4% paraformaldehyde
Acknowledgements
Jinjin Guo, Mary Duah, Joe Vaughan & Diane Faria are acknowledged for their technical assistance on the GUDMAP project. JV & DF performed mouse dissection. MD was responsible for clone procurement. JG & MD performed template PCR reactions and performed hybridizations. MT Valerius designed the probes, annotated the expression patterns and managed the data.

 

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Department of Health and Human Services National Institutes of Health Contacts Citing GUDMAP National Institute of Diabetes and National Institute of Child Health and Human Development