35 results about "Hypothetical protein" patented technology

Disclosed herein are methods for diagnosing or treating pregnancy related hypertensive disorders that include the use of a polypeptide or a nucleic acid encoding a polypeptide selected from the following: follistatin related protein, interleukin 8, inhibin A, VEGF-C, angiogenin, beta fertilin, hypothetical protein, leukocyte associated Ig-like receptor secreted protein, erythroid differentiation protein, adipogenesis inhibitory factor, corticotropin releasing factor binding protein, alpha-1 anti-chymotrypsin, insulin-like growth factor binding protein-5, CD33L, cytokine receptor like factor 1, platelet derived endothelial growth factor, lysyl hydroxylase isoform 2, stanniocalcin precursor, secreted frizzled related protein, galectin-3, alpha defensin, ADAM-TS3, cholecystokinin precursor, interferon stimulated T-cell alpha chemoattractant precursor, azurocidin, sperminine oxidase, UDP glycosyltransferase 2 family polypeptide B28, neurotrophic tyrosine kinase receptor 2, neutral endopeptidase, CDC28 protein kinase regulatory subunit 2, beta glucosidase, lanosterol synthase, calcium/calmodulin-dependent serine protein kinase, estrogen receptor-alternatively spliced transcript H, chemokine (CX3C motif) receptor 1, tyrosinase-related protein 1, hydoxy-delta-5-steroid dehyrogenase, dihydropyramidinase-like-4, and cytochrome P450-family 11.

The invention is directed to vaccine compositions and methods based on P. gingivalis proteins identified to be regulated by haem availability that can be used in the prevention and treatment of periodontal disease. In particular, two specific internalin-like P. gingivalis proteins, namely PG0350 and PG1374 involved in the internalization of P. gingivalis by host cells, the hypothetical protein, PG1019 purported to be a cell surface lipoprotein and the alkyl hydroperoxide reductase protein, PG0618 have been identified as useful targets for the prevention and treatment of periodontal disease.

The invention relates to recombinant protein of A1S_1523 as well as a preparation method and application of the recombinant protein. The recombinant protein comprises A1S_1523 mature peptide, and an amino acid sequence of the recombinant protein is shown in SEQ ID NO. 3. The recombinant protein disclosed by the invention is high in expression quantity and convenient to separate and purify, is efficient and safe, can be directly matched with adjuvants for use, and can be used for preparing acinetobacter baumannii infection resistant subunit vaccines and related detection kits; proven by animal experiments, gene engineering recombinant monovalent subunit vaccines have good immune protective effects on acinetobacter baumannii infection resistance; and the recombinant protein can be used for laying a foundation for further researching combined vaccines and multi-subunit fusion vaccines, and can also play important roles in the development and application of prevention and treatment vaccines and diagnostic kits.

Transcript profiles for irradiated and non-irradiated P. falciparum sporozoites were compared in an attempt to identify transcripts that are reproducibly perturbed by irradiation. Four loci were identified with high confidence. Three of these transcripts were derived from 3 different known gene families, and the fourth from a gene encoding a conserved hypothetical protein of unknown function. All four loci are up-regulated in radiation attenuated sporozoites which have been shown to be very effective in establishing protective immunity against malaria. Up-regulation of these transcripts contributes directly to protective immunity. The polypeptides encoded by the transcripts, individually and/or in combination, are incorporated into subunit vaccines, useful for the prevention of malaria and the establishment of protective immunity against malaria.

The invention provides a method of diagnosing tuberculosis (TB) in a test subject, said method comprising: (i) providing expression data of two or more markers in a subject, wherein at least two of said markers are selected from transthyretin, neopterin, C-reactive protein (CRP), serum amyloid A (SAA), serum albumin, apoliopoprotein-A1 (Apo-A1), apolipoprotein-A2 (Apo-A2), hemoglobin beta, haptoglobin protein, DEP domain protein, leucine-rich alpha-2-glycoprotein (A2GL) and hypothetical protein DFKZp667I032; and (ii) comparing said expression data to expression data of said marker from a group of control subjects, wherein said control subjects comprise patients suffering from inflammatory conditions other than TB, thereby determining whether or not said test subject has TB.

The invention belongs to the technical field of molecular biology, provided are a specific gene of Acinetobacter baumannii and primers and applications thereof, the specific gene is hypothetical protein, the nucleotide sequence of which is shown as SEQ ID NO:5, and the PCR amplification primer pair is designed, the upstream primer is shown as SEQ ID NO:1, and the downstream primer is shown as SEQID NO:2; loop-mediated isothermal amplification primers, outbound primers as shown in SEQ ID NO:1 and SEQ ID NO:2, and inbound primers as shown in SEQ ID NO:3 and SEQ ID NO:4; the primers were used todetect Acinetobacter baumannii by PCR or loop-mediated isothermal amplification. The method has the advantages of accurate detection of environmental samples, convenience, good specificity and high sensitivity.

The invention discloses a bovine mycoplasma hypothetical protein MbovP732 and application thereof. The bovine mycoplasma hypothetical protein MbovP732 has an amino acid sequence as shown in the sequence table SEQ ID NO:1, and a gene encoding the protein has a nucleotide sequence as shown in the sequence table SEQ ID NO:2. The bovine mycoplasma hypothetical protein MbovP732 has reactogenicity and immunogenicity, can specifically react with bovine mycoplasma wild strains, and cannot react with vaccine strains, therefore, the bovine mycoplasma hypothetical protein MbovP732 can be used for distinguishing infection of the bovine mycoplasma wild strains from immunization of the vaccine strains.

The invention discloses a method for detecting Escherichia coli on basis of a specific gene of Escherichia coli. The specific gene of Escherichia coli is a hypothetical protein gene which has been registered in Genbank under the registration number 13702648; the specific gene widely exists in Escherichia coli, and has no obvious similarity with other species; and the specific gene has the characteristics of intraspecific commonality and interspecific specificity. Four primers, including a pair of external primers B3 and F3 as well as a pair of internal primers BIP and FIP, are designed on basis of the gene; and then, the primers are applied in loop-mediated isothermal amplification (LAMP), and the external primers B3 and F3 are further applied in polymerase chain reaction (PCR). The nucleotide sequence of the primers is shown in SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3 and SEQ ID NO: 4. Identification systems of two kinds of Escherichia coli, namely a PCR reaction system and a LAMP reaction system, are established according to the primers involved; and thus, the identification systems have the characteristics of being good in specificity, high in sensitivity, rapid and reliable indetection result as well as easy to operate. The detection method of Escherichia coli is used for detecting Escherichia coli in water, foods, beverages and cosmetics.

The present invention first obtains coarse exciton with rice blast germ mycelium as material and through culturing, freezing-thawing, homogenating, centrifuging and PM-10 membrance ultrafiltering, and then obtain the new rice blast germ glucoprotein exciton through further freezing-thawing and serial chromatographic purifications. The rice blast germ glucoprotein exciton has molecular weight 49.08 kDa, isoelectric point 6.01 and silver staining electrophoresis purity. Mass spectroscopic identification shows that the exciton is rice blast germ MG05155.4 open reading frame coded hypothetical protein MG05155.4. The exciton has stable property, relatively high induction on Phe deaminase activity in non-compatible interactive rice line and lowest effective concentration of 1.5 nmol/L for inducing rice peroxidase. The present invention has excellent application foreground in the biological prevention and control of rice blast.

The invention discloses a hypothetical protein gene of fasciola hepatica. Meanwhile, the invention further provides colloidal gold immunochromatography test paper prepared from the hypothetical protein gene of the fasciola hepatica. A fasciola hepatica infection detection colloidal gold test paper strip prepared by the hypothetical protein gene of the fasciola hepatica, the test paper has the characteristics of simplicity, convenience, easiness in operation, high sensitivity, high specificity, short time and the like and clear and visible result and is suitable for clinical field detection andlarge-scale epidemiological investigation.

The present invention relates to a method for the crystallization of protein using nanoparticles as nucleation agents. Precisely, the inventors performed the crystallization of such proteins as Bacillus subtilis YesR, chicken egg white lysozyme, bovine serum albumin, Alicyclobacillus acidocaldarius acetyl-CoA carboxylase, and Listeria monocytogenes hypothetical protein which have his-tag at amino terminal by using gold nanoparticles in diverse sizes and shapes in the presence of Ni²⁺ ions. As a result, it was confirmed that the chance of successful crystallization was higher with the gold nanoparticles than without the gold nanoparticles and the various crystallization conditions were successfully screened. Therefore, the method for inducing nucleation of the invention can be advantageously used for the disclosure of protein structure by increasing the chance of successful crystallization of protein.

A novel mammalian protein related to human hypothetical protein FLJ22662 (SEQ ID NO: 1) and homologous hypothetical proteins from mammal species other than Homo sapiens. The protein is expressed in neutrophils and is characterized as a phospholipase B of a novel family (PLB-II). The protein is characterized in comprising one or two single chain polypeptide SU subunits that are different with respect to their amino acid sequences (i.e. at least one SU1 subunit and/or at least one SU2 subunit), where the amino acid sequence of: i) SU1 comprises SEQ ID NO: 2 or a variant thereof ii) SU2 comprises SEQ ID NO: 3 or a variant thereof. There is also described an antibody preparation which is specifically directed against the mammalian protein and a method for determining the occurrence or level of an analyte in a sample. The method is characterized in that analyte is related to the mammalian protein.

The invention relates to the field of biotechnology, and discloses application of a mycobacterium tuberculosis protein. According to the application of the mycobacterium tuberculosis protein, ribose kinase, fatty acyl-AMP ligase, cystathionine beta-lyase and hypothetical protein in the mycobacterium tuberculosis protein are used as a diagnostic antigen, a corresponding antibody in a serum to be detected is detected through an indirect ELISA so as to judge whether a person to be detected is infected with mycobacterium tuberculosis or not, whether the a person to be detected is suffered tuberculosis or not is further judged, high reliability, specificity and sensitivity are achieved, and the application of a mycobacterium tuberculosis protein can be applied to the field of serological diagnosis of the tuberculosis.

The invention provides a hypothetical protein gene, a primer probe group thereof and application of the hypothetical protein gene to detection of metschinia dicuspidata, and belongs to the technical field of quantitative detection of the metschinia dicuspidata. The nucleotide sequence of the gene segment used for detecting the metschhia pastoris is as shown in SEQ ID NO.1, the nucleotide sequence of the hypothetical protein gene containing the gene segment is as shown in SEQ ID NO.2, and the primer probe group used for amplifying the gene segment is as shown in SEQ ID NO.3-5. The gene segment and the primer probe group for detecting the Meiqi yeast two-pointed, provided by the invention, have the advantages of high sensitivity, strong specificity and high detection accuracy, can be used for quantitatively detecting the quantity of the Meiqi yeast two-pointed carried in river crabs, and have important significance on prevention and control of diseases caused by the Meiqi yeast two-pointed.

The invention discloses nosema bombycis hypothetical protein NB29, a recombinant expression vector containing the nosema bombycis hypothetical protein NB29 and an application of the recombinant expression vector. A nucleotide sequence of the nosema bombycis hypothetical protein NB29 is shown in SEQ ID NO.1, expressed protein is secretory, a truncation form N3 is screened out according to the nosema bombycis hypothetical protein NB29, fusion Cas9 protein is stably expressed in silkworm cytoplasm, during infection of nosema bombycis, secretory protein NB29-B and NB29-N3 of nosema bombycis interact, Cas9 is dragged in a host cell nucleus, and the purpose of host gene editing is achieved. The Cas9 medicated inducible gene editing vector can stably edit host genes, a new idea is provided for preparing insect nosema bombycis death causing models and nosema bombycis control, reference is provided for control of nosema bombycis and other pathogens capable of infecting humans, and meanwhile, afoundation is laid for functional research of related genes.

The invention provides a gene related to protein hydrolysis capacity and a screening method for lactobacillus helveticus with high protein hydrolysis capacity based on the gene, and belongs to the technical field of molecular biology. According to the invention, a whole-genome correlation analysis technology is adopted for rapid screening so as to obtain a coding hypothetical protein gene relatedto lactobacillus helveticus proteolytic activity. The hypothetical protein gene regulates and controls the proteolysis capacity of lactobacillus helveticus in a negative regulation and control mode, and can be used as a molecular marker for detecting the proteolysis activity of lactobacillus helveticus to be applied to screening of lactobacillus helveticus strains. The screening work of lactobacillus helveticus strains with high protein hydrolysis capacity is greatly simplified, and a new thought is provided for the strain screening work.