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Joint Conference on Digital Libraries and cDNA Libraries

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Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease

Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease

April 7, 2021March 8, 2021 Elsie Anderson
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.
Role of T cell immune response cDNA 7 on the pathology of acute graft-versus-host disease
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.

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.

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.

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.

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.

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.

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

Human Uterus Tumor lysate

HTL-1384 Alpha Diagnostics 1 mg
EUR 773

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.

CAT/ Rat CAT ELISA Kit

ELA-E0242r Lifescience Market 96 Tests
EUR 886

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 siRNA

20-abx900807 Abbexa
  • EUR 551.00
  • EUR 732.00
  • 15 nmol
  • 30 nmol

CAT siRNA

20-abx910366 Abbexa
  • EUR 551.00
  • EUR 732.00
  • 15 nmol
  • 30 nmol

CAT siRNA

20-abx910367 Abbexa
  • EUR 551.00
  • EUR 732.00
  • 15 nmol
  • 30 nmol

CAT Antibody

1-CSB-PA070043 Cusabio
  • EUR 222.00
  • EUR 195.00
  • 100ug
  • 50ug
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
  • EUR 317.00
  • EUR 244.00
  • 100ul
  • 50ul
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
  • EUR 317.00
  • EUR 244.00
  • 100ul
  • 50ul
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
  • EUR 222.00
  • EUR 195.00
  • 100ug
  • 50ug
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
  • EUR 597.00
  • EUR 333.00
  • 150ul
  • 50ul
Description: A polyclonal antibody against CAT. Recognizes CAT from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC

pCas9- CAT

PVT11001 Lifescience Market 2 ug
EUR 301

pOTB7-CAT

PVT18217 Lifescience Market 2 ug
EUR 231

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
  • EUR 565.00
  • EUR 481.00
  • 100 rxns × 20 ul Systems
  • 50 rxns × 20 ul Systems

Novo? cDNA Kit

M1165-100 Biovision
EUR 354

Novo? cDNA Kit

M1165-25 Biovision
EUR 267

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

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
  • EUR 732.00
  • EUR 398.00
  • 150 ul
  • 50 ul

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.
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A cDNA analysis disclosed the discordance of genotype-phenotype correlation in a patient with attenuated MPS II and a 76-base deletion in the gene for iduronate-2-sulfatase
RNA-cDNA hybrids mediate transposition via different mechanisms
June 2022
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Flame Photometry Standards - Measurement and Industies https://youtu.be/HzUjXE3KKjw via @YouTube #Chemistry #Standards #Measurement

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Viscosity CM Short Webinar from @Reagecon https://youtu.be/abhiaYkxDNE via @YouTube #measurement #standards #Science #Viscosity

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12 Apr 2021

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