Abstract: Providing web search results which are verifiable via the blockchain may offer transparency into valid web pages and their availability when conducting a search. One example method of operation may include performing a plurality of web page interactions by a plurality of network node devices operating on a network, validating existence of valid web pages, detecting invalid web pages based on the plurality of web page interactions, and storing a valid page package with the valid web pages in a blockchain.

Abstract: The invention discloses a polypeptide compound and a preparation method and application thereof. The polypeptide compound has a structural formula as follows: (XAXBXCXDXE-X)2KY, or {(XAXBXCXDXE-X)2K}2KY, or {({XAXBXCXDXE-X}2K)2K}2KY, where, XA is a polar amino acid molecule, XB and XE are alkaline amino acid molecules (the same or different), XC and XD are non-polar amino acid molecules (the same or different), K is lysine (Lys, K), and X and Y are null, or any one or more amino acid or chemical groups. The polypeptide compound provided in the invention has an effect of enhancing the immune function of a body and has an application potential of being developed into a clinical medicine capable of enhancing the immune function of a body.

Abstract: According to one or more embodiments of the present invention, a computer-implemented method for shortening just-in-time compilation time includes creating a first container for executing a first computer program, the execution comprising generating, using a just-in-time compiler, a compiled code for a first code-portion of the first computer program. The method further includes storing the compiled code for the first code-portion in a code-share store. The method further includes creating a second container for executing a second computer program comprising a second code-portion. The method further includes determining that the second code-portion matches the first code-portion, and in response retrieving the compiled code from the code-share store for executing the second computer program.

Abstract: The present invention discloses a polypeptide compound, a method for preparing the polypeptide compound, and an application of the polypeptide compound. The polypeptide compound is represented by a structural formula A-(A-K)n-Y, n being a natural number; wherein A is a short peptide fragment with biological activity; K is lysine Fmoc-Lys (Dde)-OH that contains two active amino groups, and Y is null or any one or more amino acids or chemical groups; when n=1, the structural formula of the polypeptide compound is A-(A-K)-Y; when n=2, the structural formula of the polypeptide compound is A-(A-K)2-Y; when n=3, the structural formula of the polypeptide compound is A-(A-K)3-Y; . . . . The polypeptide compound disclosed and provided in the present invention has effects of inhibiting tumor growth and improving immune function.

Abstract: The present invention discloses a polypeptide compound, a preparation method and an application thereof. The structural formula of the polypeptide compound is (XAXBXCXDXEXFXG—X)2KY or {(XAXBXCXDXEXFXG—X)2K}2KY or {({XAXBXCXDXEXFXG—X}2K)2K}2KY, where, XA, XB, XD, XE and XG are one of aliphatic amino acid molecules respectively, XC and XF are aliphatic amino acid molecules or heterocyclic amino acid molecules, K is lysine (Lys, K), X or Y is null or any one or more amino acid or chemical groups. The polypeptide compound provided in the invention has an effect of enhancing the immune function of a body and has an application potential of being developed into a clinical medicine capable of enhancing the immune function of a body.

Abstract: The invention discloses a polypeptide compound and a preparation method and application thereof. The polypeptide compound has a structural formula as follows: (XAXBXCXDXE-X)2KY, or {(XAXBXCXDXE-X)2K}2KY, or {({XAXBXCXDXE-X}2K)2K}2KY, where, XA is a polar amino acid molecule, XB and XE are alkaline amino acid molecules (the same or different), XC and XD are non-polar amino acid molecules (the same or different), K is lysine (Lys, K), and X and Y are null, or any one or more amino acid or chemical groups. The polypeptide compound provided in the invention has an effect of enhancing the immune function of a body and has an application potential of being developed into a clinical medicine capable of enhancing the immune function of a body.

Abstract: Providing web search results which are verifiable via the blockchain may offer transparency into valid web pages and their availability when conducting a search. One example method of operation may include performing a plurality of web page interactions by a plurality of network node devices operating on a network, validating existence of valid web pages, detecting invalid web pages based on the plurality of web page interactions, and storing a valid page package with the valid web pages in a blockchain.

Abstract: A 4-copy branched peptide represented by a formula of (XA-XB-XC-XD-X1)4>(K-X2)2>K-X3. XA and XC separately represent an uncharged polar amino acid; XB and XD separately represent an alkaline amino acid; >K- represents lysine comprising two free activated amino groups for amino acid addition condensation reactions; X1 and X2 separately represents an amino acid sequence comprising between 0 and 5 random amino acids, and X1 and X2 are the same, different, or absent; and X3 is a sequence comprising between 1 and 4 random amino acids. The peptide is capable of inhibiting tumor growth and enhancing immunity.

Abstract: A lithium rechargeable battery includes an electrode assembly that has a first electrode and a second electrode that are wound together with a separator interposed between them, a can that houses the electrode assembly, and a heat-resistant member that is positioned in between the bottom of the interior of the can and the electrode assembly.