Microalgae biotechnologies are quickly creating into new industrial settings. A number of excessive worth merchandise exist already available on the market, and biotechnological growth is concentrated on genetic engineering of microalgae to open up future financial alternatives for meals, gas and pharmacological manufacturing. Colony-polymerase chain response (colony-PCR or cPCR) is a essential methodology for screening genetically reworked microalgae cells.

Nonetheless, the power to quickly display screen 1000’s of transformants utilizing the present colony-PCR methodology, turns into a really laborious and time-consuming course of. Herein, the non-homologous transformation of Chlamydomonas reinhardtii utilizing the electroporation and glass beads strategies generated greater than seven thousand transformants. With a purpose to handle this spectacular variety of clones effectively, we developed a high-throughput screening (HTS) cPCR methodology to quickly maximize the detection and choice of positively reworked clones. For this, we optimized the Chlamydomonas reworked cell format on the tradition media to enhance genomic DNA extraction and cPCR in 96-well plate.

The appliance of this optimized HTS cPCR methodology provides a fast, cheaper and dependable methodology for the detection and choice of microalgae transformants. Our methodology, which saves as much as 80% of the experimental time, holds promise for evaluating genetically reworked cells and choice for microalgae-based biotechnological functions akin to artificial biology and metabolic engineering.

Improvement and software of a quadruplex real-time PCR assay for differential detection of porcine circoviruses (PCV1 to PCV4) in Jiangsu province of China from 2016 to 2020

 

Up to now, 4 species of porcine circoviruses (PCVs), together with PCV1-4, have been reported to exist within the scientific circumstances. Quick and efficient differential detection is essential to observe the an infection and co-infection standing of PCVs for adopting dependable management methods. Nonetheless, at the moment obtainable strategies can’t concurrently differentiate the 4 species of PCV strains.

On this research, a quadruplex real-time PCR assay primarily based on TaqMan probes was developed for differential detection of PCV1-4. The brand new quadruplex real-time PCR assay exhibited glad specificity, sensitivity, repeatability and reproducibility. As well as, the new assay was utilized to the detection of 120 scientific samples collected from 2016 to 2020 in Jiangsu province of China and in contrast with beforehand reported PCV1-Four singleplex standard PCR assays. Based mostly on the scientific efficiency, the outcomes from the quadruplex real-time PCR and standard PCR assays confirmed 100% settlement.

A complete of 47 samples had been detected as PCV constructive by the quadruplex real-time PCR assay, together with 1, 2, 1 samples had been co-infected with PCV1 and PCV4, PCV2 and PCV3, PCV2 and PCV4, respectively. Full-length ORF2 sequencing and phylogenetic evaluation supported the real-time PCR outcomes that 5, 34, eight and Four of the 51 PCV sequences had been PCV1, PCV2, PCV3 and PCV4, respectively. This research gives a promising different device for fast differential detection of PCVs and confirms the coexistence of all species of PCV1-Four strains in Jiangsu province lately.

Allele-specific PCR with a novel information processing methodology primarily based on distinction worth for single nucleotide polymorphism genotyping of ALDH2 gene

 

Single nucleotide polymorphism (SNP) evaluation primarily based on allele-specific polymerase chain response (AS-PCR) is a comparatively efficient and economical methodology in contrast with different genotyping applied sciences akin to DNA sequencing, DNA hybridization and isothermal amplification methods. However AS-PCR is proscribed by its labor-intensive optimization of response parameters and time-consuming end result evaluation. On this research, we put ahead a novel concept of knowledge processing to handle this downside. SNP evaluation was completed by AS-PCR with endpoint electrochemical detection.

For every pattern, two separate reactions had been run concurrently with two units of allele-specific primers (wild-type primers for W system and mutant primers for M system). We measured their redox present indicators on screen-printed electrodes as soon as AS-PCR completed and calculated the distinction worth of present indicators between two techniques to find out the genotyping end result. Based mostly on the distinction worth of fluorescent indicators, real-time fluorescent PCR was used to review response parameters in AS-PCR.

With screened parameters, we obtained the genotyping outcomes inside 50 min. 36 hair-root samples from volunteers had been analyzed by our methodology and their genotypes of ALDH2 gene (encoding aldehyde dehydrogenase 2) had been completely an identical with information from commercialized sequencing. Our work first employed distinction worth between two response techniques to distinguish allele and offered a novel concept of knowledge processing in AS-PCR methodology. It is ready to promote the short evaluation of SNP within the fields of well being monitor, illness precaution, and customized analysis and therapy.

American foulbrood (AFB) and European foulbrood (EFB) are the 2 main bacterial ailments affecting honeybees, resulting in a lower in viability of the hive, reducing honey manufacturing, and leading to important financial losses to beekeepers. Because of the inefficiency and/or low efficacy of some antibiotics, researches with nanotechnology signify, probably, new therapeutic methods. Nanostructure medication have offered some advantagesover the standard medicines, akin to sluggish, gradual and managed launch, elevated bioavailability, and lowered side-effects.

On this research, totally different contaminated larvae had been collected from two apiaries; the combs that had signs of American and European foulbrood had been remoted. In vitro antimicrobial exercise of camphor tree silver nano-particles in opposition to foulbrood ailments had been characterised utilizing UV-Vis spectrophotometry and scanning electron microscope (SEM) that proves the formation of silver nanoparticles with measurement vary 160-660 nm. The antimicrobial exercise of the silver nanoparticles was examined utilizing agar diffusion assay and proved their capability to successfully stop the pathogenic bacterial progress in each AFB and EFB.

DGGE-PCR approach has been utilized for the identification of un-common bacterial infections honeybees relying on 16S rRNA amplification from their complete extracted DNA and has been recognized as Serratia marcescens (TES), deposited in GenBank with a brand new accession quantity (MT240613). The outcomes had been confirmed pressure has been detected by DGGE-PCR evaluation inflicting uniquely contaminated brood that was attacked by the American Foulbrood It could possibly be concluded that greenly synthesized silver nanoparticles is projected for use as efficient therapy for honeybee bacterial ailments. These materials want extra investigations below discipline circumstances and research the risk of its residues in honeybee merchandise akin to honey, and beeswax.

 

 

cDNA from Human Tumor Tissue: Adrenal
C1235004-10	Biochain	10 reactions	EUR 282
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 Normal Adrenal Gland Whole tissue lysate
HALX-11050	Alpha Diagnostics	1 mg	EUR 773

Bovine ADRENAL 50 EA*
57101-2	Pel-Freez	50 Each	EUR 756.65

cDNA from Human Adult Normal Tissue: Adrenal
C1234004	Biochain	40 reactions	EUR 376
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: Adrenal
C1534004	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 (Cynomolgus) Normal Tissue: Adrenal
C1534004-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.

Monkey (Cyno.) Normal Adrenal Gland Whole tissue lysate
MCL-1160	Alpha Diagnostics	1 mg	EUR 773

Monkey (Rhesus) Normal Adrenal Gland Whole tissue lysate
MRL-1267	Alpha Diagnostics	1 mg	EUR 773

cDNA from Human Diabetic Tissue: Whole Eye
C1236108Dia-10	Biochain	10 reactions	EUR 383
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 Human Adult Normal Tissue: Whole Eye
C1234108-10	Biochain	10 reactions	EUR 446
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 (Cynomolgus) Normal Tissue: Whole Eye
C1534108-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.

BAM-12P, Bovine Adrenal Medulla Docosapeptide
5-00748	CHI Scientific	4 x 1mg	Ask for price

Bovine EYE WHOLE 25 EA*
57111-2	Pel-Freez	25 EA	EUR 295.55

Bovine KIDNEY WHOLE 2 EA*
57120-2	Pel-Freez	2 EA	EUR 174.84

Bovine PITUITARY WHOLE 25 EA*
57133-2	Pel-Freez	25 EA	EUR 597.88

Adrenal Lysate
1417	ProSci	0.1 mg	EUR 191
Description: Adrenal tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. 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.

Adrenal Lysate
1470	ProSci	0.1 mg	EUR 191
Description: Adrenal tissue lysate was prepared by homogenization in modified RIPA buffer (150 mM sodium chloride, 50 mM Tris-HCl, pH 7.4, 1 mM ethylenediaminetetraacetic acid, 1 mM phenylmethylsulfonyl fluoride, 1% Triton X-100, 1% sodium deoxycholic acid, 0.1% sodium dodecylsulfate, 5 μg/ml of aprotinin, 5 μg/ml of leupeptin. 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.

Adrenal Lysate
21-160	ProSci	0.1 mg	EUR 390.5
Description: Monkey (Cynomolgus) adrenal 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 monkey (Cynomolgus) adrenal 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 adrenal tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The adrenal tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot.

Adrenal Lysate
XBL-11050	ProSci	0.1 mg	EUR 553.25
Description: Human adrenal 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 adrenal 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 adrenal tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The adrenal tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot.

Adrenal Dissociation System 9 (Adrenal), Mouse and Rat
4-20209	CHI Scientific	ea	Ask for price

Paraffin Tissue Section - Human Adrenal Tumor: Adrenal Pheochromocytoma
T2235004-2	Biochain	5 slides	EUR 257
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.

Adrenal Lupus Lysate
XBL-10316	ProSci	0.1 mg	EUR 663.5
Description: Human adrenal 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 adrenal 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 adrenal tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The adrenal tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot.

Adrenal Cytoplasmic Lysate
XBL-10453	ProSci	0.1 mg	EUR 227.75
Description: Human adrenal tissue cytoplasmic protein lysate was prepared by isolating the cytoplasmic protein from whole tissue homogenates using a proprietary technique. The human adrenal 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 adrenal tissue cytoplasmic protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated adrenal tissue cytoplasmic protein is then Western analyzed by GAPDH antibody, and the expression level is consistent with each lot.

Adrenal Membrane Lysate
XBL-10454	ProSci	0.1 mg	EUR 737
Description: Human adrenal tissue membrane protein lysate was prepared by isolating the membrane protein from whole tissue homogenates using a proprietary technique. The human adrenal 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 adrenal tissue membrane protein pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The isolated adrenal tissue membrane protein is then Western analyzed by either GAPDH or β-actin antibody to confirm there is no signal or very weak signal.

Rabbit anti Whole Bovine serum antibody (IgG fraction)
40R-RB002	Fitzgerald	20 mg	EUR 327
Description: Affinity purified Rabbit polyclonal Rabbit anti Whole Bovine serum antibody (IgG fraction)

Adrenal Dissociation System 2 (Leydig, Adrenal), Mouse and Rat
4-20202	CHI Scientific	ea	Ask for price

Rabbit Anti-Bovine IgG (whole IgG from colostrum), unlabeled
80516	Alpha Diagnostics	1 ml	EUR 202

Rabbit Anti-Bovine IgG (whole IgG from serum), unlabeled
80517	Alpha Diagnostics	1 ml	EUR 202

Pig ADRENAL 50 EA*
59401-2	Pel-Freez	50 EA	EUR 440.19

Rabbit ADRENAL 50 EA
41201-2	Pel-Freez	50 EA	EUR 341.23

Adrenal Liver Cirrhosis Lysate
XBL-10315	ProSci	0.1 mg	EUR 663.5
Description: Human adrenal 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 adrenal 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 adrenal tissue pattern on SDS-PAGE gel is shown to be consistent for each lot by visualization with coomassie blue staining. The adrenal tissue is then Western analyzed by either GAPDH or β-actin antibody, and the expression level is consistent with each lot.

Adrenal Dissociation System 4 (Heart, Adrenal chromaffin, Paraneurons), Mouse and Rat
4-20204	CHI Scientific	ea	Ask for price

Histone (Whole) Antibody
abx023918-2ml	Abbexa	2 ml	EUR 509

Rat Whole Heart
PC35133	Neuromics	P0 Rat - Whole Heart X2	EUR 1341

Mouse Whole Heart
PC35135	Neuromics	P0 Mouse - Whole heart X2	EUR 1341

Rabbit ADRENAL MATURE 50 EA
41301-2	Pel-Freez	50 EA	EUR 341.23

Total Protein from Lupus: Adrenal
P1236004Lup	Biochain	1 mg	EUR 461
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation.

Frozen Tissue Section - Lupus: Adrenal
T1236004Lup	Biochain	5 slides	EUR 474
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.

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

Whole Blood PCR Mix
M1143-200	Biovision		EUR 321

Whole Human Serum antibody
20-1727	Fitzgerald	1 L	EUR 30
Description: Goat polyclonal Whole Human Serum antibody

Whole Human Serum antibody
20-S1110G000-V0	Fitzgerald	10 ml	EUR 133
Description: Goat polyclonal Whole Human Serum antibody

CMV protein (whole cell)
30-AC70	Fitzgerald	1 ml	EUR 403
Description: Purified native CMV protein (whole cell)

Monkey IgM (whole molecule)
31R-AI093	Fitzgerald	250 µg	EUR 417
Description: Monkey whole IgM

Human adrenal cortex antibody ELISA Kit
ELA-E0342h	Lifescience Market	96 Tests	EUR 824

Total Protein from Liver Cirrhosis: Adrenal
P1236004Lcs	Biochain	1 mg	EUR 461
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation.

Frozen Tissue Section - Human Tumor: Adrenal
T1235004	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.

Paraffin Tissue Section - Human Adrenal Tumor
T2235004	Biochain	5 slides	EUR 257
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.

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.

Goat Anti-human Chorionic Gonadotropin Whole (hCG-Whole) IgG aff pure
HCG14-A	Alpha Diagnostics	1 mg	EUR 286

First-Strand cDNA Synthesis SuperMix (cDNA up to 12 kb)
20-abx09801620ulSystems	Abbexa	EUR 620.00 EUR 523.00	100 rxns × 20 ul Systems 50 rxns × 20 ul Systems

First-Strand cDNA Synthesis SuperMix (cDNA up to 15 kb)
20-abx09802120ulSystems	Abbexa	EUR 871.00 EUR 662.00	100 rxns × 20 ul Systems 50 rxns × 20 ul Systems

cDNA from Plant Normal Tissue: cDNA from Plant: Soy bean
C1634370	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 Probe Diluent Solution
AR0063	BosterBio	5mL	EUR 106

Tetro cDNA Synthesis Kit
BIO-65042	Bioline	30 Reactions	Ask for price

Tetro cDNA Synthesis Kit
BIO-65043	Bioline	100 Reactions	Ask for price

SensiFAST cDNA Synthesis Kit
BIO-65053	Bioline	50 Reactions	Ask for price

SensiFAST cDNA Synthesis Kit
BIO-65053/S	Bioline	Sample	Ask for price

SensiFAST cDNA Synthesis Kit
BIO-65054	Bioline	250 Reactions	Ask for price

Human eNOS cDNA probe
eNOS51-D-2	Alpha Diagnostics	2 ug	EUR 445

Plant Tissue cDNA: Arabidopsis
PC34-310	Alpha Diagnostics	10 rxn	EUR 415

OneScriptPlus cDNA Synthesis Kit
G235	ABM	25 x 20 ul reactions	EUR 97

OneScriptPlus cDNA Synthesis Kit
G236	ABM	100 x 20 ul reactions	EUR 169

OneScriptPlus cDNA Synthesis SuperMix
G453	ABM	25 x 20 ul reactions	EUR 97

OneScriptPlus cDNA Synthesis SuperMix
G454	ABM	100 x 20 ul reactions	EUR 169

circRNA cDNA Synthesis Kit
G627	ABM	25 rxn (20 ul/rxn)	EUR 309

Evo™ cDNA Kit
M1164-100	Biovision		Ask for price

Evo™ cDNA Kit
M1164-25	Biovision		Ask for price

Novo? Transcriptome cDNA Kit
M1167-100	Biovision		EUR 952

Novo? Transcriptome cDNA Kit
M1167-25	Biovision		EUR 441

cDNA from Arteriosclerosis: Aorta
C1236012Hd-4	Biochain	40 reactions	EUR 811
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 hypertension: Artery
C1236013Hd-2	Biochain	40 reactions	EUR 668
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 Arteriosclerosis: Artery
C1236013Hd-4	Biochain	40 reactions	EUR 811
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 hypertension: Vein
C1236020Hd-2	Biochain	40 reactions	EUR 668
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 Lupus: Colon
C1236090Lup	Biochain	40 reactions	EUR 668
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.