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Expression Database
GUDMAP:11556
Data Source
Gene
Tnfsf13b
tumor necrosis factor (ligand) superfamily, member 13b
Theiler Stage
TS23
Images
Development time: 12hrs.
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:
M Todd Valerius, Andrew P McMahon
Submitted By:
M Todd Valerius,
Harvard University, Cambridge, MA, USA, tvalerius@mcb.harvard.edu
Archive ID:
173
Submission ID:
AM_190309_21
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
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Probe
Gene:
Symbol:
Tnfsf13b
Name:
tumor necrosis factor (ligand) superfamily, member 13b
(
MGI:1344376
)
Probe ID:
maprobe:5588
Name of cDNA:
9530009N24
Additional Name of cDNA:
MSR1664
Sequence ID:
AK079180.1
5' primer sequence:
AATGACCCACCCCTGTGGTC
3' primer sequence:
TAATACGACTCACTATAGGGAGCTGAGAAGCCATGGAA
5' primer location:
316
3' primer location:
1021
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:
757
Probe Notes:
Probe template was amplified from RIKEN clone 9530009N24 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 = TAATACGACTCACTATAGGGAGCTGAGAAGCCATGGAA : Forward primer sequence= AATGACCCACCCCTGTGGTC. MSR1664.
 
 
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
Linked Publications
Linked Submissions
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.