Please translate the biochemical article, not machine translation

Using solid-state 29Si cross-polarized magic angle rotation (SDO MA) NMR spectroscopy, we confirmed that the Astragalus polysaccharide group is covalent in debt bondage to hydrotalcite, and finally forms the Oxane bond (molybdenum-silicon (Male = LDH of zinc and chromium) activity). In addition, solid-state 29si director NMR technology was applied to evaluate the properties of the silicon atom. Annotations (0,1,2,3) are used to describe the degree of crosslinking depending on the type of Mosilicon, summarized in Table 2 showing the 29Si solid-state NMR peak transfer of t-peaks previously made and the summit position of parts per million (parts per million).

10] Figure 3, 29Si mas NMR spectra and corresponding least-squares suitable AL-meter displays. The experimental spectrum is directed by the ** Orchestra and the spinning edge finger of Asterix. The orchestra can be broken down into several simulations of individual peaks.

By spectroscopic simulation, the silyl group attached to the type of oxane bond can be determined. In addition, relative proportions of Astragalus polysaccharide-modified hydrotalcite in each type of oxane bond sample could determine their relative peak intensities; A summary of these results is presented in Table 2 of the AL-M of the surface attached to the oxane bond can be the main cause of the two-tooth (tritium) and triple-tooth (T3) types. Since there is no interference with the Deschamps anion in the Al-M system, most of the ethoxy group of Astragalus polysaccharides appear to form oxane bonds hydroxyl groups.

Microorganisms, especially yeast, have been used in the production of beer, wine, and other fermented products for thousands of years. However, it wasn't until 1878 that the yeast cells in yeast that were really responsible for fermentation were named enzymes. Less than twenty years later, the inanimate nature of enzymes was clearly demonstrated with years of cell-free extracts that can convert glucose into ethanol.

In 1926, through the purification and crystallization of urease, it was finally proved that enzymes are proteins.

Absolutely hand-flipped, but there are some places that you can delete at your own discretion

Because I studied biology in English, there may be a little bit of a mistake in the use of proper vocabulary

Microorganisms, especially yeast, have been used for thousands of years in the production of beer, wine, and other fermented products. However, it was not until 1878 that the substances actually responsible for the fermentation of yeast cells were called enzymes, and less than twenty years later, enzymes in the non-animal kingdom were clearly confirmed to extract cells and be able to catalyze the conversion of glucose into ethanol. In 1926, the purification and crystallization of enzyme proteins and urease were finally demonstrated.

Microorganisms, especially yeast, have been used for thousands of years to produce beer, wine, and other fermented products. However, until 1878 the actual parts of yeast cells responsible for fermentation were rated as enzymes less than twenty years after the naturally occurring enzymes were clearly demonstrated, extracting cells free of years capable of catalyzing the conversion of glucose into ethanol. Finally, it was demonstrated that the enzyme protein was purified and crystallized with urease in 1926.

Effect of GC polymorphisms on plasma IL-6 levels and muscle strength in older women within the catalyst range of the interleukin-6 gene.

2.Passivation of capsaicin-sensitive nerves slows lung remodeling in Gini pigs with chronic hypersensitivity pneumonitis.

3.Enhanced inhibition of murine prostate cancer proliferation by immunization or medication of active human umbilical cord vascular endothelial cells and CRM197.

4.The local least-squared discriminant analysis method was used to classify the 1hmrs of brain mass extracts into high-decomposition classification.

5.Use Greek patterns and rhythms to influence the perception of home and non-home emotions.

6.Anti-inflammatory and analgesic effects of lovastatin on rodents in vivo and in vivo.

1。-174 g C affects polymorphisms in the promoter region of genes on plasma IL-6 interleukin-6 levels and muscle strength in older women.

2。Live in capsaicin-sensitive reduces chronic allergic lung inflammation in pulmonary artery reconstructions in guinea pigs.

3。Enhancement of inhibred inbreeding of prostate cancer with viable immunization or administration of human umbilical vein endothelial cells and CRM197

4。Classified brain tumors were extracted from high-resolution spectra using partial least squares discriminant analysis.

5。Greek patterns and rhythmic manipulation affect the perception of emotions by home and nonmusicians.

6。In vivo and in vitro anti-inflammatory, anti-nociceptive lovastatin in active rodents.

1.Effect of interleukin-6 (IL-6) gene promoter-174 g C polymorphism on plasma IL-6 content and muscle strength in older women.

2.Inactivation of capsaicin-sensitive nerves reduces lung remodeling in guinea pigs with chronic reactive pneumonia.

Others can be logged in below**.

Xinda Medical Translation.

RNA recognition is determined by embryonic cell and germ cell totipotency factors fatedeterminant Mexico-3

Reconstitution of germ cells, totipotent stem cells, and early embryonic development of cell differentiation rely on post-transcriptional regulatory mechanisms.

However, nucleotide sequence specificity and Mexican-3 mRNA recognition requirements remain unclear.

Only a few candidates have been targeted for regulation, and the extent to which the Mexico3 target network is adequate is unknown.

Here, we define the consensus sequence Mexican-3 RNA recognition requirements and show that this element is regulated by the Mexican-3 gene that is dependent on the needs of living worms.

On this basis, we identified several candidates with the goal of Mexico-3, which helps to explain the dual role in regulating the norm of totipotent cell fate of germ cells and embryonic stem cells.

RNA identification embryonic cells Fatedeterminant and germline studies mex-3 factors.

Newer totipotent stem cells rely on stress regulatory mechanisms in germline and early embryonic differentiation.

However, nucleotide sequence specificity and requirements for mRNA recognition of MEX-3 are not well understood.

Only a few candidate regulatory goals have been identified, and the goals of the maximum MEX-3 network are unknown.

Here, we will identify and indicate for the MEX-3 consensus sequence that this RNA element is required for MEX-3-dependent gene expression regulation by a live parasite.

On this basis, we identified several candidates whose work was aimed at helping to interpret the specifications of its mex-3 specification dual role in germline stem cell research and embryonic cell fate.

So many words are 20 points... I don't look at it.

。Chemical and microbiological analysis.

Analyze the concentration of diabetes and protein in the experiment.

diet, excretion and probiotic products, is based on:

1990). Root.

Bullet calorimeter for General Electric Measurement (model.

1261, Juvenile Instruments Limited, Morin, Interleukin), and chromium.

Automated spectrophotometer for concentration determination.

Total V-650, Head Office, Tokyo, Japan) in accordance with.

Fenton and Fenton (1979).

Stool samples for microbial testing (14 and 28).

and intestinal chyme (28).

Determination of total anaerobic for different media.

bacteria (pancreatic soy agar), bifidobacteria. (Agar), lactobacilli. (Liu Jian agar + sodium azide + cystine.)

hydrochloride monohydrate), (Tableau agar) and Clostridium spp.

Coliform bacteria (purple red bile agar). Detection of microorganisms.

Probiotic products were cultured by technology.

For Lactobacillus acidophilus is enumerated the use of agar+

Sodium azide + cystine hydrochloride monohydrate, Bacillus subtilis.

Plate counting agar with agar, Saccharomyces cerevisiae and Aspergillus spergillus.

Glucose agar. Determination of anaerobic conditions.

Anaerobic is caused by the use of gas anaerobic systems.

barrel, No. 260678; Medium, Detroit, m). Trypsin soy agar (No.

236950), agar (No. 288130), purple-red bile agar (No. 288130).

216695), plate counting agar (No. 247940), and potato glucose.

Agar (No. 213400) was used to purchase it from the agar laboratory.

Detroit, m), with Taiwan Sugar Agar (CM0589).

Egg whites (New Hampshire, UK). value of probiotic products.

Determined values (basic table lifting, sewing machine, Germany).

Small intestinal morphology. Three cross-sections for each intestinal sample.

Prepare after dyeing, azurean and use standards.

Paraffin embedding procedure. A total of 10 complete, welloriented fluff units were selected in triplicate each.

Intestinal cross-section as previously described (Kim et al. ，2008）。Villi height is measured from the fluff of an iceberg.

The villous crypt junction, and the definition of crypt depth is:

Deeply depressed adjacent villi. All forms.

Measurements (villus height and crypt depth).

Image processing is used in 10-meter increments.

Analysis system (Optimus Prime software version, **cybergenetics, North Reading, MA).

I change 100 points to 100RMB. **This is the price、

The "linear discriminant analysis" method was used to evaluate the highest resolution (i.e., the best**) of the three ratios of the four cell lines (1,3,28,29). We take a step-by-step approach to linear discriminant analysis. First, we analyze each polymer individually, assessing the potential high peaks of each polymer based on its ability to resolve (or**) four cell lines.

Each analysis was performed with 32 observations (4 cell lines x 8 replicates) with 4 variables (cell line indicators and 3 wavelength variables for emission intensity). This "linear discriminant analysis" step confirms that the optimal strength is 410 nm for P2 polymer and 420 nm for P1 polymer.

English Cattle Troupe].

LDA (lithium diisopropyl amine) should be used to evaluate the three cell lines that provide the greatest disambiguity (i.e., the best ** device). (its number is ), we are at the forefront of the times. First, we applied each individual LDA polymer, and we evaluated each potential peak when differentiating (or**) four cell lines based on their ability.

Each assay involves 32x magnification observations (i.e., 4 cell lines 8 replicates) and 4 variables (cell line indicators and three emission intensity wavelength variables). This step is to determine the optimal analytical protocol for the P2 polymer with an LDA strength of 410 nm and the P1 polymer with a strength of 420 nm.

Lasers are suitable for evaluation, and these three ratios provide maximum discrimination (i.e., best**) between cell lines. (1,3,28,29) We apply lasers in a gradual fashion. First, we used linear discriminant analysis for each polymer separately, and we evaluated each potential peak capacity based on the distinction (or**) of the four cell lines.

All of these analyses were performed using 32 observations (4 cell lines with 8 replicates) and 4 variables (cell line indicators and three wavelength variables for emission intensity). This laser analysis step determines the optimal intensity of 410 nm for dipolymers and 420 nm for small polymers.

The LDA should be used to assess these three ratios (i.e., those that provide the greatest discrimination. , the best ** device) between the cell lines We apply in the gradual fashion LDA.

First, we applied each individual LDA polymer and we evaluated each potential peak based on its ability to distinguish (or) four cell lines. Each assay was performed using 32 observations (4 cell lines, 8 replicates) and 4 variables (cell line indicators and three emission intensity wavelength variables). This step determines the 410 nm P2 polymer and 420 nm P1 polymer for the best analytical LDA strength.