Transcriptome profiling and weighted gene co-expression network analysis of early floral development in Aquilegia coerulea

The first phases of floral development include a number of crucial processes that form the basis of the subsequent morphogenesis of floral organs and reproductive success. Currently, the main changes in transcription during this development window have been characterized in the model species Arabidopsis Thaliana, but it is known to know how the dynamics of transcription changes during these development processes in others Plant systems.

Here we led the first profile of in-depth transcriptome in anticipated floral development in aquilegia with four steps of finely dissected development, with eight biological replicas per floor. Use of the analysis of the expression of differential gene and analysis of the weighted gene co-expression network, we have identified the two crucial genes whose expression changes brand transitions between the development steps and the hub genes in Co-expression modules. Our results support the potential functional conservation of key genes at the beginning of floral development that have been identified in other systems, but also reveal a number of unknown or neglected lockers worthy of a further investigation.

In addition, our results highlight not only the dynamics of transcriptional regulation during early floral development, but also the potential involvement of key networks of small RNA and post-translational regulations at these development stages. In the case of a mass radiological or nuclear scenario, it is important to distinguish between non-exposed individuals (worried), low-dose and those who develop the acute hematology radiation syndrome (HARS) in the Three first days postulated. In previous Baboine studies, we identified changes in expression of modified genes after irradiation, which predicted the severity of the severity of the severe subsequent. Similar changes in the expression of four of these genes have been observed using a human human human blood model in vitro. However, these studies provided only limited information on the deadline for changes after exposure to HAR development relations.

Identify the mechanisms underlying the protective effect of tetramethylpyrazine against intitro ototoxicity induced by cisplatin in Hei-Oc1 hearing cells using gene expression profiling

Sensorinal auditory loss is widespread in patients receiving cisplatin therapy. Tetramethylpyrazine (TET) and Tanhinone IIa (TAN IAA) have protective roles against hearing impairment or ototoxicity. This study was intended to study the molecular mechanisms underlying the otoxicity induced by cisplatin and the protective effect of TET and TAN IIA against it. Corti Organ House Ear Institute 1 Hearing cells was treated with titrant doses of Tan IIa, Tet and Cisplatin. In a dosage of cell viability, cisplatin, tanning IIa and TET had IC50 values ​​of 42.89 μm, 151.80 and 1.04×103 mg / l, respectively.

TAN II Cytotoxicity induced by increased cisplatin. However, Tet <75 mg / L concentrations have attenuated cytotoxicity and cisplatin-induced apoptosis. In addition, a sequencing analysis of the RNA was carried out on hearing cells treated for 30 h with a cisplatin of 30 μm alone for 48 hours or combined with 37.5 mg / l tt for 30 h. The genes expressed differentially (DEGS) induced under these conditions have been identified and examined using the ontology of genes and the kyoto encyclopedia of genes and an analysis of the genomes trails. Cisplatin has increased the expression of P53 and Foxo-related genes, such as the FAS, P21 / CDKN1A and BCL-2 link component, but decreased the expression of the insulin-type growth factor (IGF1), as well as Genes in clusters histones (histon) 1 and hist2. Treatment with the Foxo3 and BCL-2 connecting component Tet 3, and increased the expression of the IGF1. In addition, Tet Tet Genes surregulated associated with WNT signaling, but not to genes related to P53. Thus, the otoprotective TET properties can be mediated by activating WNT and IgF1 signaling and the inhibition of Foxo signaling.

 Transcriptome profiling and weighted gene co-expression network analysis of early floral development in Aquilegia coerulea
Transcriptome profiling and weighted gene co-expression network analysis of early floral development in Aquilegia coerulea

Ladder identification and phylogenetic and expression profiling analyzes, XE gene families in Brassica Rapa L. and Brassica oleracea l

Background: xyloglucan endotransglucosylase / hydrolase genes (XTHS) is a multigen family and play key roles in the regulation of cell wall scalability in growth and plant development. Brassica Rapa and Brassica Oleracea contain XTHES, but a detailed identification and characterization of the fifteenth family of these species, as well as the analysis of their tissue expression profiles, have not been carried out before.

Results: In this study, 53 and 38 Xth Genes have been identified in B. Rapa and B. Oleracea respectively, which contained new members not observed in previous studies. All XTHS of B. Rapa, B. Oleracea and Arabidopsis Thaliana could be classified into three groups, group I / II, III and the Early Diverging Group on the basis of phylogenetic relations. Gene structures and patterns of motifs were similar within each group. All XTHES in this study contained two retained domains characteristic (glyco_hydro and xet_c). The XTHS are located mainly in the cell wall, but some are also located in the cytoplasm.

The analysis of the genes expansion mechanisms revealed that genome triplication events of the entire genome (WGT) and Duplication Tandem (TD) may have been the main mechanisms representing the expansion of the XIENTE GENE FAMILY. Interestingly, TD genes all belonged to the I / II group, suggesting that TD was the main reason for the largest number of genes in these groups. B. OLERACEA had lost more than 10th genes, the domain retained Xet_C and the exudix of active site pattern stored compared to B. Rapa, in accordance with the asymmetric evolution between the two genomes of Brassica. A majority of Xth Genes have presented different tissue-specific expression models based on RNA-SEQ data analyzes. In addition, there was a differential expression of Xth of duplicate genes in both species, indicating that their functional differentiation occurred after B. Rapa and B. Oleracea diverged from a common ancestor.

Monkey Ovary Total Protein, Rhesus

UT-406 0.5mg
EUR 176

Monkey Rhesus Ovary Genomic DNA

UG-406 0.1mg
EUR 210

Monkey Cynomolgus Ovary Genomic DNA

KG-406 0.1mg
EUR 210

Monkey Ovary cDNA-Random Primer, Cynomolgus

KD-406-RH 30 reactions
EUR 316

cDNA - Monkey (Rhesus) Normal Tissue: Ovary

C1534183 40 reactions
EUR 1311

cDNA - Monkey (Cynomolgus) Normal Tissue: Ovary

C1534183-Cy 40 reactions
EUR 1311

Normal Rhesus Monkey Ovary (5 slides/pack, single section/slide)

S-RsFPT166 1 unit
EUR 95

Ovary Lysate

21-468 0.1 mg
EUR 468.6
Description: Rat ovary tissue lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The rat ovary tissue total protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the ovary tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The ovary tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot.

Pig Ovary cDNA

PD-406 30 reactions
EUR 243

Rat Ovary cDNA

RD-406 30 reactions
EUR 243

Sheep Ovary cDNA

SD-406 30 reactions
EUR 243

Bovine Ovary cDNA

BD-406 30 reactions
EUR 243

Rabbit Ovary cDNA

TD-406 30 reactions
EUR 243

ovary Tissue block

15 1 unit
EUR 535

Chicken Ovary cDNA*

CD-406 30 reactions
EUR 243

Hamster Ovary cDNA

AD-406 30 reactions
EUR 243

BOVINE, OVARY, FRESH

8600840 1EA
EUR 74.42

MiniPig Ovary cDNA

ND-406 30 reactions
EUR 446

Ovary Lupus Lysate

XBL-10370 0.1 mg
EUR 1117.5
Description: Human ovary tissue lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The human ovary tissue total protein is provided in a buffer including HEPES (pH7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the ovary tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The ovary tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot.

Fetal Ovary Lysate

XBL-10414 0.1 mg
EUR 890.7
Description: Fetal human ovary tissue lysate was prepared by homogenization using a proprietary technique. The tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The fetal human ovary tissue total protein is provided in a buffer including HEPES (pH7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, Sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the ovary tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The ovary tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot.

PORCINE, OVARY, FRESH

8604940 1EA
EUR 67.09

BOVINE, OVARY, FROZEN

8620840 1EA
EUR 74.42

PORCINE, OVARY, FROZEN

8624940 1EA
EUR 67.09

OORA00483-10U - OVARY

OORA00483-10U 1Each
EUR 55

OORA00483-1EA - OVARY

OORA00483-1EA 1Each
EUR 59

Ovary Membrane Lysate

XBL-10768 0.1 mg
EUR 991.5
Description: Human ovary tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human ovary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated ovary tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated ovary tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal.

Chicken Ovary Sections

CP-406 10 slides
EUR 240

Ovary Cytoplasmic Lysate

XBL-10767 0.1 mg
EUR 273.3
Description: Human ovary tissue cytoplasmic protein lysate was prepared by isolating the cytoplasmic protein from whole tissue homogenates using a proprietary technique. The human ovary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The cytoplasmic protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, glycerol, and a cocktail of protease inhibitors. For quality control purposes, the isolated ovary tissue cytoplasmic protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated ovary tissue cytoplasmic protein is then Western analyzed by GAPDH antibody, and the expression level is consistent with each lot.

Rat Ovary Total RNA

RR-406 0.025mg
EUR 160

Pig Ovary Total RNA

PR-406 0.1mg
EUR 160

Mouse CD1 Ovary cDNA

MD-406 30 reactions
EUR 243

Mouse BLC Ovary cDNA

MD-406-BLC 30 reactions
EUR 280

Mouse C57 Ovary cDNA

MD-406-C57 30 reactions
EUR 280

Cat Ovary Genomic DNA

FG-406 0.1mg
EUR 210

Dog Ovary Genomic DNA

DG-406 0.1mg
EUR 210

Guinea Pig Ovary cDNA

GD-406 30 reactions
EUR 243

Rat Ovary Genomic DNA

RG-406 0.1mg
EUR 177

Sheep Ovary Total RNA

SR-406 0.1mg
EUR 160

Human Ovary Total RNA

HR-406 0.025mg
EUR 229

Pig Ovary Genomic DNA

PG-406 0.1mg
EUR 177

Rat Ovary 1 Month Total Protein

RT-406-M1 1mg
EUR 177

Bovine Ovary Total RNA

BR-406 0.1mg
EUR 160

Rabbit Ovary Total RNA*

TR-406 0.05mg
EUR 160

Hamster Ovary Total RNA*

AR-406 0.05mg
EUR 160

Chicken Ovary Total RNA*

CR-406 0.05mg
EUR 160

Rat Ovary Tissue Lysate

LYSATE0011 200ug
EUR 180
Description: This cell lysate is prepared from rat ovary tissue using Boster's RIPA Lysis Buffer (AR0105) using a standard whole cell lysate protocol. The concentration was determined using the BCA assay process and then diluted using Dithiothreitol (DTT) and a reducing SDS sample loading buffer, heated for 5 minutes at 100˚C.

Rat Ovary Total Protein

RT-406 0.5mg
EUR 153

Rat Ovary Tissue Lysate

IRTOVTL100UG each
EUR 804
Description: Rat Ovary Tissue Lysate

MiniPig Ovary Total RNA

NR-406 0.1mg
EUR 319

Pig Ovary Total Protein

PT-406 1mg
EUR 153

Mouse Ovary Genomic DNA

MG-406 0.05mg
EUR 177

Sheep Ovary Genomic DNA

SG-406 0.1mg
EUR 177

Rat Ovary 12 Months Total Protein

RT-406-M12 1mg
EUR 177

Rat Ovary 2 Months Total Protein

RT-406-M2 1mg
EUR 177

Rat Ovary 3 Months Total Protein

RT-406-M3 1mg
EUR 177

Rat Ovary 6 Months Total Protein

RT-406-M6 1mg
EUR 177

Bovine Ovary Genomic DNA

BG-406 0.1mg
EUR 177

Equine Ovary Genomic DNA

GE-406 0.1mg
EUR 210

Rabbit Ovary Genomic DNA

TG-406 0.1mg
EUR 177

Human Ovary Tumor lysate

HTL-1333 1 mg
EUR 927.6

OORA00539-1U - Rat OVARY

OORA00539-1U 1Each
EUR 60

Ovary Tissue Slide (Normal)

11-201-10um 10 um
EUR 241.8

Ovary Tissue Slide (Normal)

11-201-4um 4 um
EUR 216.6

Ovary Tissue Slide (Benign)

11-202-10um 10 um
EUR 241.8

Ovary Tissue Slide (Benign)

11-202-4um 4 um
EUR 216.6

Hamster Ovary Genomic DNA

GA-406 0.1mg
EUR 177

Cat Ovary Frozen Sections

FF-406 10 slides
EUR 261

Chicken Ovary Genomic DNA

GC-406 0.1mg
EUR 177

Dog Ovary Frozen Sections

DF-406 10 slides
EUR 261

Mouse Ovary Tissue Lysate

LYSATE0015 200ug
EUR 180
Description: This cell lysate is prepared from mouse ovary tissue using Boster's RIPA Lysis Buffer (AR0105) using a standard whole cell lysate protocol. The concentration was determined using the BCA assay process and then diluted using Dithiothreitol (DTT) and a reducing SDS sample loading buffer, heated for 5 minutes at 100˚C.

Rat Ovary Frozen Sections

RF-406 10 slides
EUR 228

Sheep Ovary Total Protein

ST-406 1mg
EUR 153

Human Ovary Total Protein

HT-406 0.5mg
EUR 176

Human Ovary Tissue Lysate

IHUOVTL100UG each
EUR 245
Description: Human Ovary Tissue Lysate

OORA00539-1EA - Rat OVARY

OORA00539-1EA 1Each
EUR 59

Pig Ovary Frozen Sections

PF-406 10 slides
EUR 261

Total Protein - Lupus: Ovary

P1236183Lup 1 mg
EUR 913

Bovine Ovary Total Protein

BT-406 1mg
EUR 153

Rabbit Ovary Total Protein

TT-406 1mg
EUR 153

Ovary Tissue Slide (Abnormal)

11-210-10um 10 um
EUR 241.8

Ovary Tissue Slide (Abnormal)

11-210-4um 4 um
EUR 216.6

Dog Ovary paraffin Sections

DP-406 10 slides
EUR 240

Chicken Ovary Total Protein

CT-406 1mg
EUR 153

Cat Ovary Paraffin Sections

FP-406 10 slides
EUR 240

Hamster Ovary Total Protein

AT-406 1mg
EUR 153

Rat Ovary Paraffin Sections

RP-406 10 slides
EUR 228

Human Ovary Frozen Sections

HF-406 10slides
EUR 240

OORA00510-1U - Rabbit OVARY

OORA00510-1U 1Each
EUR 255

MiniPig Ovary Total Protein

NT-406 1mg
EUR 176

Pig Ovary Paraffin Sections

PP-406 10 slides
EUR 240

Sheep Ovary Frozen Sections

SF-406 10 slides
EUR 261

Ovary Membrane Tumor Lysate

XBL-10777 0.1 mg
EUR 752.1
Description: Human ovary tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human ovary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The membrane protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, Glycerol, sodium deoxycholate, NP-40, and a cocktail of protease inhibitors. For quality control purposes, the isolated ovary tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated ovary tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal.

Mouse Ovary Nuclear Extract

X12012 500 µg Ask for price

Bovine Ovary Frozen Sections

BF-406 10 slides
EUR 261

Rabbit Ovary Frozen Sections

TF-406 10 slides
EUR 240

OORA00510-1EA - Rabbit OVARY

OORA00510-1EA 1Each
EUR 239

Rat WS Ovary Total RNA

RR-406-WS 0.025mg
EUR 160

Hamster Ovary Frozen Sections

AF-406 10 slides
EUR 240

Chicken Ovary Frozen Sections

CF-406 10 slides
EUR 261

Sheep Ovary Paraffin Sections

SP-406 10 slides
EUR 240

Human Ovary Paraffin Sections

HP-406 10 slides
EUR 228

MiniPig Ovary Frozen Sections

NF-406 10 slides
EUR 344

OORA00457-10U - Hamster OVARY

OORA00457-10U 1Each
EUR 75

OORA00457-1EA - Hamster OVARY

OORA00457-1EA 1Each
EUR 69

Bovine Ovary Paraffin Sections

BP-406 10 slides
EUR 240

OCPB00134-100UG - Ovary Lysate

OCPB00134-100UG 0.1mg
EUR 139

OCPB00449-100UG - Ovary Lysate

OCPB00449-100UG 0.1mg
EUR 409

Fetal Ovary Cytoplasmic Lysate

XBL-10773 0.1 mg
EUR 273.3
Description: Human ovary tissue cytoplasmic protein lysate was prepared by isolating the cytoplasmic protein from whole tissue homogenates using a proprietary technique. The fetal human ovary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The cytoplasmic protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, glycerol, and a cocktail of protease inhibitors. For quality control purposes, the isolated ovary tissue cytoplasmic protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated ovary tissue cytoplasmic protein is then Western analyzed by GAPDH antibody, and the expression level is consistent with each lot.

Ovary Cytoplasmic Tumor Lysate

XBL-10776 0.1 mg
EUR 273.3
Description: Human ovary tissue cytoplasmic protein lysate was prepared by isolating the cytoplasmic protein from whole tissue homogenates using a proprietary technique. The human ovary tissue was frozen in liquid nitrogen immediately after excision and then stored at -70°C. The cytoplasmic protein is provided in a buffer including HEPES (pH 7.9), MgCl2, KCl, EDTA, Sucrose, glycerol, and a cocktail of protease inhibitors. For quality control purposes, the isolated ovary tissue cytoplasmic protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated ovary tissue cytoplasmic protein is then Western analyzed by GAPDH antibody, and the expression level is consistent with each lot.

Hamster Ovary Paraffin Sections

AP-406 10 slides
EUR 228

MiniPig Ovary Paraffin Sections

NP-406 10 slides
EUR 344

Mouse CD1 Ovary Total RNA

MR-406 0.025mg
EUR 160

Mouse C57 Ovary Total RNA

MR-406-C57 0.025mg
EUR 180

Guinea Pig Ovary Total RNA*

GR-406 0.05mg
EUR 160

Mini Pig Ovary Genomic DNA

GN-406 0.1mg
EUR 210

Rat WS Ovary Total Protein

RT-406-WS 0.5mg
EUR 153

Ovary adenocarcinoma tissue array

OV1502 each
EUR 258
Description: Ovary adenocarcinoma tissue array, including TNM and pathology grade, 75 cases/150 cores

Ovary adenocarcinoma tissue array

OV20814 each
EUR 546
Description: Ovary adenocarcinoma tissue array, including TNM and pathology grade, 208 cases/208 cores, replacing OV2084

Ovary adenocarcinoma tissue array

OV2161 each
EUR 474
Description: Ovary adenocarcinoma tissue array, including TNM and pathology grade, 216 cases/216 cores

Cancer of the ovary, 102 cases (1.5mm)

OVC1021 1
EUR 300
Description: Ovary cancer tissue array, 102 cases of normal/benign (5 cases) and cancer (97 cases) tissues with grading and TNM staging data.

Cancer of the ovary, 228 cases (1.1mm)

OVC2281 1
EUR 552
Description: Ovary cancer tissue array containing 8 cases of normal/benign conditions and 220 cases of cancers with grading and TNM staging data.

59429-2 PIG OVARY 25 EA*

59429-2 25 EA
EUR 1979

Mouse Balbc Ovary Total RNA

MR-406-BLC 0.025mg
EUR 180

Guinea Pig Ovary Genomic DNA

GG-406 0.1mg
EUR 177

Rat WS Ovary Frozen Sections

RF-406-WS 10 slides
EUR 228

Ovary Western Blot, 14 species

AW-406 1 Blot
EUR 1031

cDNA - Human Tumor Tissue: Ovary

C1235183-10 10 reactions
EUR 578

Human Ovary cDNA-Oligo-dT

HD-406 30 reactions
EUR 280

Mouse CD1 Ovary Total Protein

MT-406 0.5mg
EUR 153

Mouse BLC Ovary Total Protein

MT-406-BLC 0.5mg
EUR 180

Mouse C57 Ovary Total Protein

MT-406-C57 0.5mg
EUR 180

Monkey Anti-Ovary Antibody,AOAb ELISA Kit

E01A71284 96T
EUR 700
Description: ELISA

Monkey Anti-Ovary Antibody,AOAb ELISA kit

E09A2099-192T 192 tests
EUR 1524
Description: A sandwich ELISA for quantitative measurement of Monkey Anti-Ovary Antibody,AOAb in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.

Monkey Anti-Ovary Antibody,AOAb ELISA kit

E09A2099-48 1 plate of 48 wells
EUR 624
Description: A sandwich ELISA for quantitative measurement of Monkey Anti-Ovary Antibody,AOAb in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.

Monkey Anti-Ovary Antibody,AOAb ELISA kit

E09A2099-96 1 plate of 96 wells
EUR 822
Description: A sandwich ELISA for quantitative measurement of Monkey Anti-Ovary Antibody,AOAb in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.

41229-2 RB OVARY Y 50 EA

41229-2 50 EA
EUR 263

Guinea Pig Ovary Total Protein

GT-406 0.5mg
EUR 153

Rat WS Ovary Paraffin Sections

RP-406-WS 10 slides
EUR 228

Rat Ovary cDNA-Random Primer

RD-406-RH 30 reactions
EUR 243

Ovary Tumor Tissue Array - 12 cases of ovary cancer paired with adjacent normal tissues

Z7020087 5 slides
EUR 1657.2
Description: Our tissue products are produced by strictly following the IRB ethical standards and procedures and from highest quality tissues. Immediately after collection the tissues are placed in liquid nitrogen and examined by certified pathologists. The thickness of each individual section is ~5um. They are Hematoxylin and Eosin stained and quality tested by immunostaining with anti-beta-actin antibodies. Our tissue products are suitable for various studies on cellular level (RNA localization, Protein expression, etc.) on both normal and pathological cases. It is also an excellent control and educational tool.

Human Ovary Fetal Tissue Lysate

IHUOVFSTL100UG each
EUR 1676
Description: Human Ovary Fetal Tissue Lysate

Human Lupus Ovary Tissue Lysate

IHUOVLUPPTL100UG each
EUR 1939
Description: Human Lupus Ovary Tissue Lysate

Human Ovary Tumor Tissue Lysate

IHUOVTLT100UG each
EUR 361
Description: Human Ovary Tumor Tissue Lysate

Mouse CD1 Ovary Frozen Sections

MF-406 10 slides
EUR 228

Mouse BLC Ovary Frozen Sections

MF-406-BLC 10 slides
EUR 253

Mouse C57 Ovary Frozen Sections

MF-406-C57 10 slides
EUR 253

Human Ovary cDNA-Random Primer

HD-406-HR 30 reactions
EUR 280

Guinea Pig Ovary Frozen Sections

GF-406 10 slides
EUR 240

OORA00427-10U - GUINEA PIG OVARY

OORA00427-10U 1Each
EUR 80

OORA00427-1EA - GUINEA PIG OVARY

OORA00427-1EA 1Each
EUR 79

Mouse CD1 Ovary Paraffin Sections

MP-406 10 slides
EUR 228

Conclusions: We conducted the first systematic analysis of different genes families in B. Rapa and B. Oleracea. The results of this survey can be used for reference in other studies on the functions of the Xth Genes and the evolution of this multigen family.