Activation of T lymphocytes is the initiating issue of the incidence of acute graft-versus-host illness (aGVHD), and cytotoxic T lymphocyte antigen-4 (CTLA-4) is the inhibitory receptor for activating T cells. T cell immune response cDNA 7 (TIRC7) is taken into account an upstream regulator of CTLA-4; nevertheless, little is known concerning the results of TIRC7 on the regulation of CTLA-Four in aGVHD.
The aim of the current examine was to guage the regulatory results of TIRC7 on aGVHD, primarily within the pathology. Recipient mice had been uncovered to a preconditioning dose of seven.5 Gy irradiation on the day of the transplantation and had been divided into the next teams: Clean management group, bone marrow transplantation management group, whole physique irradiation group, mild-moderate aGVHD group and extreme aGVHD group.
Based on the completely different administration of CTLA-Four and TIRC7 monoclonal antibodies, the mild-moderate and extreme aGVHD teams had been randomly divided into the hematopoietic stem cell transplantation (HSCT) and HSCT + CTLA-4/TIRC7 teams. Recipient mice had been sacrificed at completely different time factors post-HSCT for histopathological evaluation by hematoxylin and eosin staining.
In contrast with the management and different experimental teams, the mice within the mixed CTLA-Four and TIRC7 group exhibited ameliorated pathological damage, and decrease pathology scores of the liver, lung and gut. These information revealed that intraperitoneal injection of anti-TIRC7 and/or anti-CTLA-Four monoclonal antibody into mice may successfully alleviate the severity of aGVHD.
Development of a cDNA expression library in a binary vector utilizing a nicking enzyme
Ligation-independent cloning (LIC), equivalent to Gibson Meeting, tends to supply clones with out an insert, relying on the sequences current on the ends of linearized vectors. We used a nicking enzyme-mediated LIC (NE-LIC) technique to assemble a cDNA library in a binary vector pER8.
Previous to setting up the cDNA library, pilot experiments had been carried out, through which the GUS coding sequence was cloned into pER8 utilizing NE-LIC. Roughly 12% of enter vector DNAs had been transformed to plasmids carrying a GUS insert, and no plasmids with out an insert had been detected, indicating that this technique is very efficient for cloning with the binary vector pER8. Subsequently, NE-LIC was adopted to assemble a cDNA library in pER8, through the use of cDNA that was PCR-amplified from a library constructed in one other vector. Because of this, a cDNA library in pER8 was efficiently constructed. Throughout library building, it is very important exclude plasmids with out an insert, since contamination from plasmids with out inserts decreases the effectivity of screening. Subsequently, NE-LIC is helpful for the development of cDNA libraries.
Growth of a Full-Size Infectious Cdna Clone of the Grapevine Berry Interior Necrosis Virus
Grapevine berry inside necrosis virus (GINV) belongs to the genus Trichovirus within the household Betaflexiviridae. The GINV isolate LN_BETA_RS was obtained from a “Beta” grapevine (Vitis riparia × Vitis labrusca) exhibiting chlorotic mottling and ring spot in Xingcheng, Liaoning Province, China. To confirm the correlation between GINV and grapevine chlorotic mottling and ring spot illness, we constructed an infectious cDNA clone of GINV isolate LN_BETA_RS utilizing the seamless meeting strategy.
Utilized therapies of agroinfiltration infectious cDNA confirmed systemic GINV an infection of the Nicotianaoccidentalis 37B by reverse transcription polymerase chain response (RT-PCR) and transmission electron microscopy, exhibiting chlorotic mottling signs on leaves. Infectious cDNA was additionally transmitted to new wholesome N. occidentalis crops by way of rub-inoculation. Furthermore, the cDNA clone was agroinfiltrated into “Beta” and “Thompson Seedless” grapevine plantlets, and the inoculated grapevines exhibited leaf chlorotic mottling and ringspot throughout the two years of statement.
GINV-inoculated “Beta” grapevines had severe leaf chlorotic mottling and ringspot signs on the entire plant, whereas comparatively few signs had been noticed on the leaves of agroinoculated “Thompson Seedless” grapevines in early spring and solely weak ring spot regularly appeared later within the prime younger leaves. Our experiments fulfilled Koch’s postulates and revealed the causative function of GINV in grapevine chlorotic mottling and ring spot illness.
A pressure of porcine deltacoronavirus: genomic characterization, pathogenicity and its full-length cDNA infectious clone
As a novel enteropathogenic coronavirus, porcine deltacoronavirus (PDCoV) warrants additional investigation. On this examine, a Chinese language PDCoV pressure, designated CHN-HN-1601, was remoted from the feces of a diarrheic piglet. After plaque purification, the genome was decided which shared 97.5%-99.5% nucleotide identities with 71 consultant PDCoV strains out there within the GenBank. The pathogenic properties of CHN-HN-1601 had been evaluated utilizing 5-day-old piglets.
All inoculated piglets developed extreme diarrhea from 2 days post-infection (dpi) onwards. To our shock, two intervals of diarrhea ranging from 2 to 7 dpi and from 13 to 19 dpi had been noticed in affected piglets throughout the experiment. Fecal viral shedding of the inoculated piglets was detected by real-time RT-PCR, with viral shedding peaked at Four and 16 dpi, respectively. At necropsy at 5 dpi, the primary gross lesions included clear, thin-walled and gas-distended intestines containing yellow watery contents.
Additional histopathological examinations, together with hematoxylin and eosin staining, immunohistochemistry, RNAscope in situ hybridization revealed that the virus an infection induced extreme villous atrophy of the small intestines, with PDCoV antigen and RNA primarily distributed within the cytoplasm of the villous epithelial cells of jejunum and ileum in piglets. The dynamic manufacturing of PDCoV-specific IgG and neutralizing antibodies in serum of the affected piglets was additionally assessed utilizing an entire virus-based ELISA and an immunofluorescence assay-based neutralization check, respectively.
 Normal Tissue: Uterus: Cervix) cDNA from Monkey (Cynomolgus) Normal Tissue: Uterus: Cervix |
|
C1534275-Cy |
Biochain |
40 reactions |
EUR 540 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 Normal Tissue: Uterus: Corpus) cDNA from Monkey (Rhesus) Normal Tissue: Uterus: Corpus |
|
C1534276 |
Biochain |
40 reactions |
EUR 540 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 Normal Tissue: Uterus: Fundus) cDNA from Monkey (Rhesus) Normal Tissue: Uterus: Fundus |
|
C1534278 |
Biochain |
40 reactions |
EUR 540 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 ELISA Kit) Human Catalase (CAT) ELISA Kit |
|
DLR-CAT-Hu-48T |
DL Develop |
48T |
EUR 441 |
|
|
|
Description: A sandwich quantitative ELISA assay kit for detection of Human Catalase (CAT) in samples from serum, plasma, tissue homogenates or other biological fluids. |
Human Catalase (CAT) ELISA Kit |
|
DLR-CAT-Hu-96T |
DL Develop |
96T |
EUR 570 |
|
|
|
Description: A sandwich quantitative ELISA assay kit for detection of Human Catalase (CAT) in samples from serum, plasma, tissue homogenates or other biological fluids. |
 ELISA Kit) Mouse Catalase (CAT) ELISA Kit |
|
DLR-CAT-Mu-48T |
DL Develop |
48T |
EUR 527 |
|
|
|
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Catalase (CAT) in samples from serum, plasma, tissue homogenates or other biological fluids. |
Mouse Catalase (CAT) ELISA Kit |
|
DLR-CAT-Mu-96T |
DL Develop |
96T |
EUR 688 |
|
|
|
Description: A sandwich quantitative ELISA assay kit for detection of Mouse Catalase (CAT) in samples from serum, plasma, tissue homogenates or other biological fluids. |
 ELISA Kit) Rat Catalase (CAT) ELISA Kit |
|
DLR-CAT-Ra-48T |
DL Develop |
48T |
EUR 549 |
|
|
|
Description: A sandwich quantitative ELISA assay kit for detection of Rat Catalase (CAT) in samples from serum, plasma, tissue homogenates or other biological fluids. |
Rat Catalase (CAT) ELISA Kit |
|
DLR-CAT-Ra-96T |
DL Develop |
96T |
EUR 718 |
|
|
|
Description: A sandwich quantitative ELISA assay kit for detection of Rat Catalase (CAT) in samples from serum, plasma, tissue homogenates or other biological fluids. |
Human Catalase (CAT) ELISA Kit |
|
RD-CAT-Hu-48Tests |
Reddot Biotech |
48 Tests |
EUR 436 |
Human Catalase (CAT) ELISA Kit |
|
RD-CAT-Hu-96Tests |
Reddot Biotech |
96 Tests |
EUR 601 |
Mouse Catalase (CAT) ELISA Kit |
|
RD-CAT-Mu-48Tests |
Reddot Biotech |
48 Tests |
EUR 533 |
Mouse Catalase (CAT) ELISA Kit |
|
RD-CAT-Mu-96Tests |
Reddot Biotech |
96 Tests |
EUR 740 |
Rat Catalase (CAT) ELISA Kit |
|
RD-CAT-Ra-48Tests |
Reddot Biotech |
48 Tests |
EUR 557 |
Rat Catalase (CAT) ELISA Kit |
|
RD-CAT-Ra-96Tests |
Reddot Biotech |
96 Tests |
EUR 775 |
Human Catalase (CAT) ELISA Kit |
|
RDR-CAT-Hu-48Tests |
Reddot Biotech |
48 Tests |
EUR 455 |
Human Catalase (CAT) ELISA Kit |
|
RDR-CAT-Hu-96Tests |
Reddot Biotech |
96 Tests |
EUR 629 |
Mouse Catalase (CAT) ELISA Kit |
|
RDR-CAT-Mu-48Tests |
Reddot Biotech |
48 Tests |
EUR 557 |
Mouse Catalase (CAT) ELISA Kit |
|
RDR-CAT-Mu-96Tests |
Reddot Biotech |
96 Tests |
EUR 774 |
Rat Catalase (CAT) ELISA Kit |
|
RDR-CAT-Ra-48Tests |
Reddot Biotech |
48 Tests |
EUR 583 |
Rat Catalase (CAT) ELISA Kit |
|
RDR-CAT-Ra-96Tests |
Reddot Biotech |
96 Tests |
EUR 811 |
 Uterus Lysate |
|
1317 |
ProSci |
0.1 mg |
EUR 191 |
|
Description: Uterus tissue lysate was prepared by homogenization in lysis buffer (10 mM HEPES pH7.9, 1.5 mM MgCl2, 10 mM KCl, 1 mM ethylenediaminetetraacetic acid, 10% glycerol, 1% NP-40, and a cocktail of protease inhibitors). Tissue and cell debris was removed by centrifugation. Protein concentration was determined with Bio-Rad protein assay. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
 Uterus Tumor Lysate |
|
1384 |
ProSci |
0.1 mg |
EUR 254 |
|
Description: Uterus tumor tissue lysate was prepared by homogenization in lysis buffer (10 mM HEPES pH7.9, 1.5 mM MgCl2, 10 mM KCl, 1 mM ethylenediaminetetraacetic acid, 10% glycerol, 1% NP-40, and a cocktail of protease inhibitors). Tissue and cell debris was removed by centrifugation. The product was boiled for 5 min in 1 x SDS sample buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 50 mM DTT. |
 Fetal Uterus Lysate |
|
XBL-10431 |
ProSci |
0.1 mg |
EUR 527 |
|
Description: Fetal human uterus 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 uterus 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 uterus tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The uterus tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot. |
 Uterus Membrane Lysate |
|
XBL-11023 |
ProSci |
0.1 mg |
EUR 516.5 |
|
Description: Human uterus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human uterus 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 uterus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated uterus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
 Bovine UTERUS 5 EA* |
|
57153-2 |
Pel-Freez |
5 EA |
EUR 204.2 |
) Uterus Tissue Slide (Normal) |
|
11-401-10um |
ProSci |
10 um |
EUR 201.5 |
Uterus Tissue Slide (Normal) |
|
11-401-4um |
ProSci |
4 um |
EUR 180.5 |
) Uterus Tissue Slide (Benign) |
|
11-402-10um |
ProSci |
10 um |
EUR 201.5 |
Uterus Tissue Slide (Benign) |
|
11-402-4um |
ProSci |
4 um |
EUR 180.5 |
) Uterus Tissue Slide (Adenocarcinoma) |
|
11-404-10um |
ProSci |
10 um |
EUR 201.5 |
Uterus Tissue Slide (Adenocarcinoma) |
|
11-404-4um |
ProSci |
4 um |
EUR 180.5 |
) Uterus Tissue Slide (Abnormal) |
|
11-419-10um |
ProSci |
10 um |
EUR 201.5 |
Uterus Tissue Slide (Abnormal) |
|
11-419-4um |
ProSci |
4 um |
EUR 180.5 |
) Uterus Tissue Slide (Adenomyoma) |
|
11-432-10um |
ProSci |
10 um |
EUR 201.5 |
Uterus Tissue Slide (Adenomyoma) |
|
11-432-4um |
ProSci |
4 um |
EUR 180.5 |
 Uterus Membrane Tumor Lysate |
|
XBL-11031 |
ProSci |
0.1 mg |
EUR 626.75 |
|
Description: Human uterus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human uterus 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 uterus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated uterus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
 Uterus-Corpus Membrane Lysate |
|
XBL-11037 |
ProSci |
0.1 mg |
EUR 516.5 |
|
Description: Human uterus-corpus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human uterus-corpus 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 uterus-corpus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated uterus-corpus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
 Uterus-Fundus Membrane Lysate |
|
XBL-11040 |
ProSci |
0.1 mg |
EUR 516.5 |
|
Description: Human uterus-fundus tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human uterus-fundus 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 uterus-fundus tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated uterus-fundus tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal. |
 Total RNA from Human Adult Normal Tissue: Uterus: Cervix of uterus |
|
R1234275-50 |
Biochain |
50 ug |
EUR 178 |
|
Description: Can be used for various studies in the realm of gene expression and regulation, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 Total RNA from Human Adult Normal Tissue: Uterus: Corpus of Uterus |
|
R1234276-10 |
Biochain |
10 ug |
EUR 194 |
|
Description: Can be used for various studies in the realm of gene expression and regulation, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 Rabbit UTERUS Y 25 EA* |
|
41253-2 |
Pel-Freez |
25 EA |
EUR 318.39 |
 Total RNA from Lupus: Uterus |
|
R1236274Lup-50 |
Biochain |
50 ug |
EUR 351 |
|
Description: Can be used for various studies in the realm of gene expression and regulation, both normal and pathological. It is an excellent control and suitable for educational purposes. |
) Uterus Tissue Slide (Endometrioid Adenocarcinoma) |
|
11-405-10um |
ProSci |
10 um |
EUR 201.5 |
Uterus Tissue Slide (Endometrioid Adenocarcinoma) |
|
11-405-4um |
ProSci |
4 um |
EUR 180.5 |
 CAT Antibody |
|
36312-100ul |
SAB |
100ul |
EUR 252 |
CAT Antibody |
|
1-CSB-PA070043 |
Cusabio |
|
|
|
|
|
Description: A polyclonal antibody against CAT. Recognizes CAT from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: IHC, ELISA;IHC:1/100-1/300.ELISA:1/20000 |
CAT Antibody |
|
1-CSB-PA599838 |
Cusabio |
|
|
|
|
|
Description: A polyclonal antibody against CAT. Recognizes CAT from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;ELISA:1:2000-1:5000, WB:1:500-1:2000, IHC:1:50-1:200 |
CAT Antibody |
|
1-CSB-PA942303 |
Cusabio |
|
|
|
|
|
Description: A polyclonal antibody against CAT. Recognizes CAT from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;ELISA:1:1000-1:2000, WB:1:200-1:1000, IHC:1:50-1:200 |
CAT Antibody |
|
1-CSB-PA004980 |
Cusabio |
|
|
|
|
|
Description: A polyclonal antibody against CAT. Recognizes CAT from Human. This antibody is Unconjugated. Tested in the following application: WB, ELISA;WB:1/500-1/2000.ELISA:1/20000 |
CAT Antibody |
|
1-CSB-PA004563GA01HU |
Cusabio |
|
|
|
|
|
Description: A polyclonal antibody against CAT. Recognizes CAT from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC |
 CAT antibody |
|
10R-3584 |
Fitzgerald |
100 ul |
EUR 726 |
|
Description: Mouse monoclonal CAT antibody |
CAT antibody |
|
10R-3585 |
Fitzgerald |
100 ul |
EUR 691 |
|
Description: Mouse monoclonal CAT antibody |
CAT antibody |
|
70R-16187 |
Fitzgerald |
50 ul |
EUR 435 |
|
Description: Rabbit polyclonal CAT antibody |
CAT antibody |
|
20C-CR1111RP |
Fitzgerald |
500 ul |
EUR 262 |
|
Description: Rabbit polyclonal CAT antibody |
 Cat IgM |
|
31C-CH0213 |
Fitzgerald |
1 mg |
EUR 392 |
|
Description: Purified Cat IgM |
 Total RNA from Human Adult Normal Tissue 5 Donor Pool: Uterus: Cervix of uterus |
|
R1234275-P |
Biochain |
50 ug |
EUR 328 |
|
Description: Can be used for various studies in the realm of gene expression and regulation, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 cDNA Synthesis SuperMix |
|
20-abx09801420ulSystems |
Abbexa |
|
- 100 rxns × 20 ul Systems
- 50 rxns × 20 ul Systems
|
|
|
 Evo? cDNA Supermix |
|
M1168-100 |
Biovision |
|
EUR 381 |
Evo? cDNA Supermix |
|
M1168-25 |
Biovision |
|
EUR 267 |
 Novo? cDNA Supermix |
|
M1169-100 |
Biovision |
|
EUR 441 |
Novo? cDNA Supermix |
|
M1169-25 |
Biovision |
|
EUR 289 |
 Frozen Tissue Section - Human Tumor: Uterus |
|
T1235274 |
Biochain |
5 slides |
EUR 338 |
|
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. |
) Uterus Tissue Slide ( Papillary serous Adenocarcinoma) |
|
11-407-10um |
ProSci |
10 um |
EUR 201.5 |
Uterus Tissue Slide ( Papillary serous Adenocarcinoma) |
|
11-407-4um |
ProSci |
4 um |
EUR 180.5 |
) Uterus Tissue Slide (Spindle Cell Tumor) |
|
11-418-10um |
ProSci |
10 um |
EUR 201.5 |
Uterus Tissue Slide (Spindle Cell Tumor) |
|
11-418-4um |
ProSci |
4 um |
EUR 180.5 |
 cDNA from Plant Normal Tissue: cDNA from Plant: Arabidopsis |
|
C1634310 |
Biochain |
40 reactions |
EUR 621 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 cDNA from Plant Normal Tissue: cDNA from Plant: Corn |
|
C1634330 |
Biochain |
40 reactions |
EUR 621 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 cDNA from Plant Normal Tissue: cDNA from Plant: Orange |
|
C1634340 |
Biochain |
40 reactions |
EUR 621 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 cDNA from Plant Normal Tissue: cDNA from Plant: Potato |
|
C1634350 |
Biochain |
40 reactions |
EUR 621 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 cDNA from Plant Normal Tissue: cDNA from Plant: Rice |
|
C1634360 |
Biochain |
40 reactions |
EUR 621 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 cDNA from Plant Normal Tissue: cDNA from Plant: Wheat |
|
C1634390 |
Biochain |
40 reactions |
EUR 621 |
|
Description: Can be used for various studies in the realm of gene expression, both normal and pathological. It is an excellent control and suitable for educational purposes. |
 PKA CAT Antibody |
|
abx147539-100ug |
Abbexa |
100 ug |
EUR 439 |
|
|
 Antibody) Catalase (CAT) Antibody |
|
20-abx132110 |
Abbexa |
-
EUR 272.00
-
EUR 592.00
-
EUR 314.00
-
EUR 154.00
-
EUR 230.00
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
|
Catalase (CAT) Antibody |
|
20-abx132122 |
Abbexa |
-
EUR 300.00
-
EUR 718.00
-
EUR 384.00
-
EUR 154.00
-
EUR 244.00
|
- 100 ug
- 1 mg
- 200 ug
- 20 ug
- 50 ug
|
|
|
Catalase (CAT) Antibody |
|
20-abx125619 |
Abbexa |
-
EUR 411.00
-
EUR 592.00
-
EUR 182.00
-
EUR 314.00
|
- 100 ul
- 200 ul
- 20 ul
- 50 ul
|
|
|
Catalase (CAT) Antibody |
|
20-abx125620 |
Abbexa |
-
EUR 411.00
-
EUR 592.00
-
EUR 182.00
-
EUR 314.00
|
- 100 ul
- 200 ul
- 20 ul
- 50 ul
|
|
|
Catalase (CAT) Antibody |
|
20-abx111432 |
Abbexa |
|
|
|
|
 CAT Rabbit pAb |
|
A11777-100ul |
Abclonal |
100 ul |
EUR 308 |
CAT Rabbit pAb |
|
A11777-200ul |
Abclonal |
200 ul |
EUR 459 |
CAT Rabbit pAb |
|
A11777-20ul |
Abclonal |
20 ul |
EUR 183 |
CAT Rabbit pAb |
|
A11777-50ul |
Abclonal |
50 ul |
EUR 223 |
Moreover, a full-length cDNA infectious clone of CHN-HN-1601 was constructed utilizing a bacterial synthetic chromosome system. The rescued virus exhibited in vitro development and pathogenic properties much like the parental virus. Taken collectively, our examine not solely enriches the knowledge of PDCoV, but additionally offers a helpful reverse genetics platform for additional pathogenesis exploration of the virus.
