Untargeted metabolomics-like screening approach for chemical characterization and differentiation of canopic jar and mummy samples from Ancient Egypt using GC-high resolution MS.

In Historic Egypt it isn’t unusual apply to embalm ineffective our our bodies and positive internal organs to assure eternal life. The character of the embalming fluid used, notably for the preservation of organs in canopic jars, debatable.

On account of this reality, the intention of this analysis was to chemically characterize and differentiate canopic jars (n = 28) and mummy (n = 6) using gasoline chromatography – extreme choice mass spectrometry (GC-HR MS) with no new targets metabolomics paying homage to screening methodology; as part of a minimally-invasive transdisciplinary larger analysis on human tissue Historic Egypt.

Submit-analytical processing of knowledge along with deconvolution, screening in opposition to NIST 14 database of spectral and extreme choice metabolomics library, and evaluation of a constructive peak. In most of the samples the presence of conifer resin characterised by longiborneol detection along with acid derivatives abietadiene and guajacol. Beeswax, proposedly used for symbolic causes and / or as a binding agent, was detected in 10 samples. Not beforehand talked about inside the literature, nonetheless is acknowledged inside the sample set in the mean time, is a medical-related substances as a constituent of anise, salicylic acid, chamazulene and Jacobine.

By making use of a centered metabolomics such an methodology to a sample of archeology for the first time, statistical analysis of intensive potential (using every choices are acknowledged and non-identified; add as a lot as 4381 choices), which confirmed essential variations inside the chemical composition of the complete canopic jar and mummified samples using analysis principle component (PCA) and partial least squares-discriminant analysis (PLS-DA). It emphasizes the need for further intensive analysis jar eventually with the intention to interpret the findings precisely.

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Description: Clone CS1 is one of four clones to EBV. Each clone reacts with different epitopes on the hydrophilic C-terminus of the cytoplasmic domain of LMP-1. This antibody is specific to 60kDa latent membrane protein (LMP-1) encoded by the BNLF1 gene of the EBV. It stains strongly with EBV-positive lymphoblastoid cell lines and EBV infected B cell immunoblasts in infectious mononucleosis. EBV, also designated human herpesvirus 4 (HHV-4), is a member of the herpesvirus family and is one of the most common human viruses. EBV infects B cells and, though often asymptomatic, it can cause infectious mononucleosis, a disease characterized by fatigue, fever, sore throat and muscle soreness.

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Description: Clone CS1 is one of four clones to EBV. Each clone reacts with different epitopes on the hydrophilic C-terminus of the cytoplasmic domain of LMP-1. This antibody is specific to 60kDa latent membrane protein (LMP-1) encoded by the BNLF1 gene of the EBV. It stains strongly with EBV-positive lymphoblastoid cell lines and EBV infected B cell immunoblasts in infectious mononucleosis. EBV, also designated human herpesvirus 4 (HHV-4), is a member of the herpesvirus family and is one of the most common human viruses. EBV infects B cells and, though often asymptomatic, it can cause infectious mononucleosis, a disease characterized by fatigue, fever, sore throat and muscle soreness.

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Description: Clone CS2 is one of four clones to EBV. Each clone reacts with different epitopes on the hydrophilic C-terminus of the cytoplasmic domain of LMP-1. This antibody is specific to 60kDa latent membrane protein (LMP-1) encoded by the BNLF1 gene of the EBV. It stains strongly with EBV-positive lymphoblastoid cell lines and EBV infected B cell immunoblasts in infectious mononucleosis. EBV, also designated human herpesvirus 4 (HHV-4), is a member of the herpesvirus family and is one of the most common human viruses. EBV infects B cells and, though often asymptomatic, it can cause infectious mononucleosis, a disease characterized by fatigue, fever, sore throat and muscle soreness.

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Description: Clone CS2 is one of four clones to EBV. Each clone reacts with different epitopes on the hydrophilic C-terminus of the cytoplasmic domain of LMP-1. This antibody is specific to 60kDa latent membrane protein (LMP-1) encoded by the BNLF1 gene of the EBV. It stains strongly with EBV-positive lymphoblastoid cell lines and EBV infected B cell immunoblasts in infectious mononucleosis. EBV, also designated human herpesvirus 4 (HHV-4), is a member of the herpesvirus family and is one of the most common human viruses. EBV infects B cells and, though often asymptomatic, it can cause infectious mononucleosis, a disease characterized by fatigue, fever, sore throat and muscle soreness.


metrological traceability for regular reference chemical measurements help the comparability of outcomes produced by utterly totally different analysts, at assorted cases, and in separate places. Ideally, this reference is the idea of the basic objects of the Worldwide System of Fashions (SI). ISO / IEC 17025 (Clause 6.5) states that the traceability of the measurement outcomes is vital attributes analytical laboratory competence, and thus, it has develop to be compulsory in a number of industries, significantly medical and medical diagnostics

 Untargeted metabolomics-like screening approach for chemical characterization and differentiation of canopic jar and mummy samples from Ancient Egypt using GC-high resolution MS.
Untargeted metabolomics-like screening methodology for chemical characterization and differentiation of canopic jar and mummy samples from Historic Egypt using GC-high choice MS.

The pattern of chemical selection inside the sea ascidians Phallusia spp.: Anti-tumor train and inhibit the metabolic pathways of steroid biosynthesis.

The superior nature of marine biodiversity is partly accountable for the scarcity of study on Indian ascidian species, which frequently objective a small number of new biomolecules. We do centered metabolomics using gasoline chromatography mass spectrometry (GC-MS) in two species of invasive ascidian to research explicit chemical selection between Phallusia nigra and P. arabica trying to find drug-like properties and metabolic pathways.

The chemical profiling of explicit individual ascidian species obtained using GC-MS, and metabolites had been determined by attempting on the NIST library and literature info. Principal component analysis GC-MS mass spectral variables confirmed a clear discrimination of two ascidian species depends on the chemical composition and taxonomy.

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EUR 386.26
Description: This is purified Mouse monoclonal antibody against Chlamydia Trachomatis LPS for WB, ELISA.

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Description: This is purified Mouse monoclonal antibody against Chlamydia Trachomatis LPS for WB, ELISA.

Mouse antibody for Chlamydia Trachomatis LPS

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Description: This is purified Mouse monoclonal antibody against Chlamydia Trachomatis LPS for WB, ELISA.

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Description: This is purified Mouse monoclonal antibody against Chlamydia Trachomatis LPS for WB, ELISA.

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Description: This is purified Mouse monoclonal antibody against Chlamydia Trachomatis MOMP for WB, ELISA.

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Description: This is purified Mouse monoclonal antibody against Chlamydia Trachomatis MOMP for WB, ELISA.

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EUR 347.1
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EUR 373.2
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EUR 347.1
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EUR 327.53
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EUR 347.1
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EUR 347.1
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EUR 373.2
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EUR 340.57
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EUR 360.16
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EUR 373.2
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EUR 1929.4
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Chlamydia trachomatis

PR-BA1372-S 250µg
EUR 642.2
Description: native, Vero cell culture

Chlamydia trachomatis

PCR-H452-PCRH45248D PCR-H452-48D
EUR 230

Chlamydia trachomatis

PCR-H452-PCRH45296D PCR-H452-96D
EUR 312

Chlamydia trachomatis (C. trachomatis) Protein

abx670256-100g 100 µg
EUR 525

Chlamydia Trachomatis PGP3-D Protein

20-abx260188
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  • 0.5 mg
  • 100 ug
  • 1 mg

Chlamydia Trachomatis PGP3-D Protein

abx260188-20g 20 µg
EUR 950

Chlamydia Trachomatis PGP3-D Protein

abx260188-5g 5 µg
EUR 350

Chlamydia pneumoniae IgA Control Serum

C1371A 3 mL
EUR 105

Chlamydia pneumoniae IgG Control Serum

C1371G 3 mL
EUR 105

Chlamydia pneumoniae IgM Control Serum

C1371M 3 mL
EUR 105

Chlamydia trachomatis L2+

GWB-52280E 1 ml Ask for price

Chlamydia trachomatis IgA

CHLA0070 96
EUR 155

Chlamydia trachomatis IgG

CHLG0070 96
EUR 155

Chlamydia trachomatis IgM

CHLM0070 96
EUR 155

Chlamydia trachomatis IgM

GWB-88FF67 1x96 Assays Ask for price

Chlamydia trachomatis IgG

GWB-701542 1x96 Assays Ask for price

Chlamydia trachomatis IgA

GWB-F926AE 1x96 Assays Ask for price

Chlamydia trachomatis -HRP

GWB-F9960B 1 ml Ask for price

Recombinant Chlamydia Trachomatis PGP3-D

7-07159 100µg Ask for price

Recombinant Chlamydia Trachomatis PGP3-D

7-07160 500µg Ask for price

Recombinant Chlamydia Trachomatis PGP3-D

7-07161 1000µg Ask for price

Chlamydia trachomatis MOMP

01011-V-01mg 0,1 mg
EUR 321
Description: Chlamydia trachomatis MOMP Recombinant antigen with out transmembrane domain.

Chlamydia trachomatis MOMP

01011-V-1000ug 1000 ug
EUR 1539
Description: Chlamydia trachomatis MOMP Recombinant antigen with out transmembrane domain.

Chlamydia trachomatis -FITC

GWB-55C294 1 ml Ask for price

Chlamydia trachomatis MOMP

GWB-19468A 1 ml Ask for price

Chlamydia trachomatis -FITC

GWB-63BDAF 1 ml Ask for price

Chlamydia trachomatis -FITC

GWB-7BFDE7 1 ml Ask for price

Metabolites, lipids, macrolides and steroids contributed strongly in opposition to discrimination in every species. The outcomes of this analysis confirms that the GC-MS primarily based chemical profiling will be utilized as a software program for classification chemotaxonomic ascidian species. P. nigra extract confirmed promising anti-tumor train in opposition to colon most cancers HT29 35 pM and MCF7-breast most cancers (34.76 M) cells in distinction with P. arabica. Of the larger than 70 metabolites had been measured, 18 metabolites which could be mapped assorted channels associated to a few metabolic pathways affected and adjusted in steroid biosynthesis, the foremost bile acid biosynthesis, and steroid hormone biosynthesis observed has modified significantly (p >> 0,004, FDR <0.01).