Abstract: An encapsulation film includes: an inner layer, where the inner layer includes a thermoplastic resin; an outer layer, where the outer layer includes a thermosetting resin; and a metal layer, where the metal layer is located between the inner layer and the outer layer, the metal layer includes at least one of stainless steel, titanium alloy, or nickel alloy, a thickness of the metal layer is 10 ?m to 60 ?m, and a tensile strength of the metal layer is 300 MPa to 2000 MPa; where a ratio of a thickness of the inner layer to the thickness of the metal layer is 0.6 to 3.

Abstract: An electrode plate includes a current collector, an active material layer, and an insulation layer. The active material layer is disposed between the current collector and the insulation layer. The insulation layer includes an insulating inorganic compound, a binder, and a polymer. The polymer includes a polymer particle. A number of the polymer particles exposed in any 45 ?m×27 ?m region on a surface of the insulation layer is 2 to 60. By controlling the number of polymer particles exposed per unit area of the insulation layer to fall within the above range.

Abstract: The invention provides novel recombinant DNA molecules, compositions, and methods for selectively regulating the expression of a transcribable polynucleotide molecule or recombinant protein in a male reproductive tissue of a transgenic plant. The invention also provides transgenic plants, plant cells, plant parts, seeds, and commodity products comprising such DNA molecules and compositions.

Abstract: A binding piece includes an insulation layer, a substrate layer, and at least one binding layer stacked together; where one of the at least one binding layer forms on an outer surface of the binding piece; where 10%?L2?100%, 1.2?L1/L2?20, L1 is an elongation rate of the insulation layer, and L2 is an elongation rate of the substrate layer.

Abstract: The invention provides novel recombinant DNA molecules, compositions, and methods for selectively regulating the expression of a transcribable polynucleotide molecule or recombinant protein in a male reproductive tissue of a transgenic plant. The invention also provides transgenic plants, plant cells, plant parts, seeds, and commodity products comprising such DNA molecules and compositions.

Abstract: A battery includes a packaging shell and a battery cell. The battery cell is disposed in the packaging shell, the battery cell includes a first electrode plate, the first electrode plate includes a first empty foil area and a second empty foil area where no active material is disposed on either side of the first electrode plate. The first empty foil area is arranged on a first surface, the second empty foil area is arranged on a second surface. At least one of the first surface and the second surface is adhered to the packaging shell by a bonding member. In a width direction of the battery cell, a width of the battery cell is W, a width of the first empty foil area is W1, a width of the second empty foil area is W2, and 0?(W1+W2)/W?40%.

Abstract: The invention provides methods and compositions for selectively suppressing the expression of a recombinant protein in a male reproductive tissue of a transgenic plant. The invention also provides methods and compositions for inducing male sterility in a transgenic plant. Plants, plant cells, plant parts, seeds, and commodity products including such compositions are aspects of the invention.

Abstract: The invention provides recombinant DNA molecules useful for providing efficient expression of proteins in transgenic plants, as well as compositions and methods for using the recombinant DNA molecules. In particular embodiments, the invention provides recombinant DNA molecules and constructs comprising sequences encoding transit peptides and operably linked sequences conferring herbicide tolerance.

Abstract: An electrochemical device includes a packaging bag, an electrode assembly, and a binder. The electrode assembly is disposed in the packaging bag. The binder is configured to bond the electrode assembly to the packaging bag. The binder includes a first bonding layer, a substrate layer, and a second bonding layer that are stacked in sequence. The first bonding layer adheres to a surface of the electrode assembly. The second bonding layer adheres to a surface that is of the packaging bag and that is close to the electrode assembly. A peel strength between the first bonding layer and the electrode assembly is F1, a peel strength between the second bonding layer and the packaging bag is F2, and the peel strengths satisfy 50 N/m?F1?1000 N/m and 1?F1/F2?10. A tensile strength of the substrate layer is 100 MPa to 2000 MPa.

Abstract: An electrode plate includes a current collector and an active material layer provided on the current collector. The active material layer includes a first composite particle including a first active material particle and a first binder particle and a second composite particle including a second active material particle and a second binder particle. In a thickness direction of the active material layer, the first composite particle is closer to the current collector than the second composite particle. A quantity of the first active material particle contained in the first composite particle is greater than a quantity of the second active material particle contained in the second composite particle. Components of both the first binder particle and the second binder particle include polypropylene.

Abstract: Example systems and methods are provided for identifying genome edits in genomes based on patterns associated with joints in target sequences of the genomes. One example method includes receiving, by a computing device, a request to identify at least one edit in an output genome, where the output genome includes one or more edits to the genome and where a reference sequence is representative of an unedited version of the genome. The method also includes identifying, by the computing device, the at least one edit of the one or more edits, based on sequence reads associated with the output genome mapped to the reference sequence relative to one or more reference edit patterns and reporting, by the computing device, the identified at least one edit.

Abstract: A battery includes a packaging shell and a battery cell. The battery cell is disposed in the packaging shell, the battery cell includes a first electrode plate, the first electrode plate includes a first empty foil area and a second empty foil area where no active material is disposed on either side of the first electrode plate. The first empty foil area is arranged on a first surface, the second empty foil area is arranged on a second surface. At least one of the first surface and the second surface is adhered to the packaging shell by a bonding member. In a width direction of the battery cell, a width of the battery cell is W, a width of the first empty foil area is W1, a width of the second empty foil area is W2, and 0? (W1+W2)/W?40%.

Abstract: The invention provides recombinant DNA molecules useful for providing efficient expression of proteins in transgenic plants, as well as compositions and methods for using the recombinant DNA molecules. In particular embodiments, the invention provides recombinant DNA molecules and constructs comprising sequences encoding transit peptides and operably linked sequences conferring herbicide tolerance.

Abstract: The reported method identifies the likelihood that a heritable sequence in a plant is to be passed onto subsequent generations. One or more genome edits are introduced into a plant cell and the gnomic DNA of the resulting plant is analyzed to determine the frequency of the one or more genome edits in the sample. Edits that are present in a quantity above a reference cutoff are considered to have a high likelihood of being heritable and capable of being passed on to subsequent generations. Edits that are present in low quantities are considered to have a low likelihood of being passed on. Plants containing desirable genome edits that are likely to be heritable are then used for cultivation and propagation.

Abstract: The invention provides methods and compositions for selectively suppressing the expression of a recombinant protein in a male reproductive tissue of a transgenic plant. The invention also provides methods and compositions for inducing male sterility in a transgenic plant. Plants, plant cells, plant parts, seeds, and commodity products including such compositions are aspects of the invention.

Abstract: Pesticidal proteins exhibiting toxic activity against Lepidopteran pest species are disclosed, and include, but are not limited to, TIC7941, TIC7941PL_1, TIC7941PL_2, and TIC7941PL_3. DNA constructs are provided which contain a recombinant nucleic acid sequence encoding one or more of the disclosed pesticidal proteins. Transgenic plants, plant cells, seed, and plant parts resistant to Lepidopteran infestation are provided which contain recombinant nucleic acid sequences encoding the pesticidal proteins of the present invention. Methods for detecting the presence of the recombinant nucleic acid sequences or the proteins of the present invention in a biological sample, and methods of controlling Lepidopteran species pests using any of the TIC7941, TIC7941PL_1, TIC7941PL_2, and TIC7941PL_3 pesticidal proteins are also provided. Also disclosed are methods and compositions to improve the insecticidal activity of a pesticidal protein against an insect pest species.

Abstract: Pesticidal proteins exhibiting toxic activity against Lepidopteran pest species are disclosed, and include, but are not limited to, TIC7941, TIC7941PL_1, TIC7941PL_2, and TIC7941PL_3. DNA constructs are provided which contain a recombinant nucleic acid sequence encoding one or more of the disclosed pesticidal proteins. Transgenic plants, plant cells, seed, and plant parts resistant to Lepidopteran infestation are provided which contain recombinant nucleic acid sequences encoding the pesticidal proteins of the present invention. Methods for detecting the presence of the recombinant nucleic acid sequences or the proteins of the present invention in a biological sample, and methods of controlling Lepidopteran species pests using any of the TIC7941, TIC7941PL_1, TIC7941PL_2, and TIC7941PL_3 pesticidal proteins are also provided. Also disclosed are methods and compositions to improve the insecticidal activity of a pesticidal protein against an insect pest species.

Abstract: This invention provides molecular constructs and methods for the temporally specific control of gene expression in plants or in plant pests or pathogens. More specifically, this invention provides plant miRNA genes having novel circadian expression patterns that are useful for designing recombinant DNA constructs for temporally specific expression of at least one gene. Also provided are non-natural transgenic plant cells, plants, and seeds containing in their genome a recombinant DNA construct of this invention.

Abstract: The invention provides recombinant DNA molecules useful for providing efficient expression of proteins in transgenic plants, as well as compositions and methods for using the recombinant DNA molecules. In particular embodiments, the invention provides recombinant DNA molecules and constructs comprising sequences encoding transit peptides and operably linked sequences conferring herbicide tolerance.

Abstract: The present disclosure provides methods and compositions for generating dominant alleles using targeted editing techniques. Also provided are modified chromosomes, cells, tissues, and plants comprising modified dominant allele.