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EMAGE:4988

Dgkz diacylglycerol kinase zeta ( MGI:1278339)
TS19 (11.5 dpc)
in situ hybridisation

Data Images
EMAGE:4988
Fig3A. from [doi:10.1016/S0014-5793(98)00490-6] FEBS Lett 429(1): 109-14, Ding L; McIntyre TM; Zimmerman GA; Prescott SM, The cloning and developmental regulation of murine diacylglycerol kinase zeta. Copyright 1998 [PMID:9657393]

Expression pattern clarity: two stars
Find spatially similar wholemount expression patterns: Find spatially similar wholemount patterns
Notes:
Sense probe gave no specific staining.
Expression Pattern Description
Spatial Annotation:
EMAGE:4988Annotation colour key:  
strong strong      
gene expression moderate moderate    
gene expression weak weak        
gene expression possible possible    
gene expression not detected not detected
wholemount mapping

Download individual expression domains:
4988_wholemount_moderate_3D_1.wlz
4988_wholemount_weak_3D_1.wlz
4988_wholemount_notDetected_3D_1.wlz
4988_wholemount_strong_3D_1.wlz
(what is wlz format?)
Download all expression domains: EMAGE:4988_all_domains.zip
Find spatially similar wholemount expression patterns:  EMAGE spatially similar wholemount patterns
Morphological match to the template: one star
Text Annotation:
StructureLevelPatternNotes
trunk somite
weak weak
spinal ganglion
weak weak
limb
weak weak
Annotation Validation: EMAGE Editor
Detection Reagent
Type:in situ hybridisation probe
Identifier:Dgkz probeA
Entity Detected:Dgkz, diacylglycerol kinase zeta ( MGI:1278339)
Notes:The Dgkz probe used in this study by Ding et al., 1998 [PMID:9657393] is one of two possible probes described as follows: "The first probe was a 716-bp 3' PstI/EcoRI fragment. It was subcloned into pBluescript II and used to make digoxigenin-labeled RNA probe by in vitro transcription (Boehringer Mannheim). The second one was from the catalytic domain region of the mDGK-zeta gene. A pair of primers with T7 or T3 promoters attached was used to amplify a 558-bp mDGK-zeta cDNA fragment. Amplified PCR products were used as templates to make digoxigenin-labeled RNA probes by using an in vitro transcription kit (Boehringer Mannheim). The sequences of the primers were: 5'-CAGAGATGCAattaaccctcactaaagggaGAGTCTCGAGAAGCCAACCCAGAG-3', T3 and 5'-CCAAGCTTCtaatacgactcactatagggagaCCCTGCTCACCTGGATCCTCAG-3', T7." Editors Note: The T3 and T7 promotors are denoted here in the primer sequences in lower case.
Chemistry:RNA
Strand:antisense
Label:digoxigenin
Specimen
Organism:mouse
Strain:Swiss Webster
Age:11.5 dpc
Theiler Stage:TS19
Mutations:none (wild-type)
Preparation:wholemount
Procedures
Staining procedure:alkaline phosphatase + unspecified
General Information
Authors:Ding L; McIntyre TM; Zimmerman GA; Prescott SM, 1998 [PMID:9657393] , Indexed and Spatially Mapped by EMAGE.
Submitted by:EMAGE EDITOR, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, UK EH4 2XU
Experiment type:non-screen
References:[ doi:10.1016/S0014-5793(98)00490-6] [ PMID:9657393] Ding L, McIntyre TM, Zimmerman GA, Prescott SM 1998 The cloning and developmental regulation of murine diacylglycerol kinase zeta. FEBS Lett (429):109-14
Links: Ensembl same gene
  Allen Brain Atlas same gene
  BioGPS same gene
  International Mouse Knockout Project Status same gene
  GEISHA Chicken ISH Database same gene
  EMBL-EBI Gene Expression Atlas same gene
  BrainStars same gene
  ViBrism same gene
Data SourceEMAGE