The spatio-temporal expression pattern of a gene provides important indications to better understand its biological function. In situ hybridization (ISH) uses a labeled complementary single-stranded RNA or DNA probe to localize gene transcripts in a whole organism, a whole organ or a section of tissue. We adapted the ISH technique to the plant parasite Meloidogyne spp. (root-knot nematode) to visualize RNAs both in free-living preparasitic juveniles and in parasitic stages settled in the plant tissues. We describe each step of the probe synthesis, digoxigenin (DIG) labeling, nematode extraction from plant tissue, and ISH procedure
A protocol is described for the detection of endogenous mRNA in whole-mount tissue using antisense R...
Molecular biology techniques are being applied to an increasing number of problems in plant nematolo...
Molecular probes were designed to identify Meloidogyne species by hybridizing to unique signature se...
The spatio-temporal expression pattern of a gene provides important indications to betterunderstand ...
A method is presented for in-situ hybridization to mRNA in second-stage juveniles (J2) of the soybea...
BACKGROUND: Plant-parasitic nematodes compromise the agriculture of a wide variety of the most commo...
As a consequence of comprehensive transcriptome analysis followed by sequencing and draft assembly o...
With the advances in genomics research of the past decade, plant biology has seen numerous studies p...
Here we describe an in situ hybridization (ISH) method using Invitrogen™ ViewRNA™ ISH Tissue Assay (...
An optimized protocol is presented to visualize gene expression in the sedentary beet cyst nematode,...
In situ hybridization is a basic method in modern plant cell and molecular biology. It is used to lo...
<p>A and B: Antisense probe in a male nematode. C and D: Antisense probe in a female nematode. E: Co...
In situ RNA-RNA hybridization (ISH) is a molecular method for localization of gene transcripts at th...
Tissue specific RNA in-situ hybridization is a critical technique required for botanists to examine ...
Identifying parasitism genes encoding proteins secreted from a nematode\u27s esophageal gland cells ...
A protocol is described for the detection of endogenous mRNA in whole-mount tissue using antisense R...
Molecular biology techniques are being applied to an increasing number of problems in plant nematolo...
Molecular probes were designed to identify Meloidogyne species by hybridizing to unique signature se...
The spatio-temporal expression pattern of a gene provides important indications to betterunderstand ...
A method is presented for in-situ hybridization to mRNA in second-stage juveniles (J2) of the soybea...
BACKGROUND: Plant-parasitic nematodes compromise the agriculture of a wide variety of the most commo...
As a consequence of comprehensive transcriptome analysis followed by sequencing and draft assembly o...
With the advances in genomics research of the past decade, plant biology has seen numerous studies p...
Here we describe an in situ hybridization (ISH) method using Invitrogen™ ViewRNA™ ISH Tissue Assay (...
An optimized protocol is presented to visualize gene expression in the sedentary beet cyst nematode,...
In situ hybridization is a basic method in modern plant cell and molecular biology. It is used to lo...
<p>A and B: Antisense probe in a male nematode. C and D: Antisense probe in a female nematode. E: Co...
In situ RNA-RNA hybridization (ISH) is a molecular method for localization of gene transcripts at th...
Tissue specific RNA in-situ hybridization is a critical technique required for botanists to examine ...
Identifying parasitism genes encoding proteins secreted from a nematode\u27s esophageal gland cells ...
A protocol is described for the detection of endogenous mRNA in whole-mount tissue using antisense R...
Molecular biology techniques are being applied to an increasing number of problems in plant nematolo...
Molecular probes were designed to identify Meloidogyne species by hybridizing to unique signature se...