Abstract: The present disclosure discloses an antibody fragment library, method for preparing the library and its applications. The essential steps in construction of the library is devoid of any restriction enzyme. Emulsion based PCR has been used as an important tool for the construction and validation of the library. The method as disclosed in the present disclosure leads to construction of a library comprising at least 8 billion clones.

Abstract: Compounds and methods are provided for the treatment of pathogenic virus infections. Compositions and methods are provided for inhibiting RNA viruses.

Abstract: The present disclosure discloses a process for immobilizing polypeptides on a surface, said method comprising: (a) coating a surface with a molecule to capture biotin tagged polypeptide to obtain a coated surface; and (b) contacting at least two biotin tagged polypeptides with the coated surface of step (a) to obtain immobilized polypeptides, wherein the biotin tagged polypeptide comprises a biotin linked to a recombinant polypeptide. The present disclosure further discloses an in-vitro method for detecting at least one binder molecule in a sample, and a process for obtaining biotin tagged polypeptide.

Abstract: The present disclosure discloses an antibody fragment library, method for preparing the library and its applications. The essential steps in construction of the library is devoid of any restriction enzyme. Emulsion based PCR has been used as an important tool for the construction and validation of the library. The method as disclosed in the present disclosure leads to construction of a library comprising at least 8 billion clones.

Abstract: A system and method of configuration of link aggregation groups includes a control unit and a port coupled to the control unit and configured to couple the network switching device to a neighboring switch. The control unit is configured to transmit a probe message to the neighboring switch, receive a remote switch identifier and link aggregation group (LAG) identifier from the neighboring switch, determine whether the remote switch identifier matches a previously received remote switch identifier and the remote LAG identifier matches a previously received remote LAG identifier. When both match, determine a first LAG associated with the previously received remote switch identifier and the previously received remote LAG identifier and assign the port to the first LAG. When both do not match, to create a second LAG, assign the port to the second LAG, and associate the remote switch identifier and the remote LAG identifier with the second LAG.

Abstract: A system and method of configuration of link aggregation groups includes a control unit and a port coupled to the control unit and configured to couple the network switching device to a neighboring switch. The control unit is configured to transmit a probe message to the neighboring switch, receive a remote switch identifier and link aggregation group (LAG) identifier from the neighboring switch, determine whether the remote switch identifier matches a previously received remote switch identifier and the remote LAG identifier matches a previously received remote LAG identifier. When both match, determine a first LAG associated with the previously received remote switch identifier and the previously received remote LAG identifier and assign the port to the first LAG. When both do not match, to create a second LAG, assign the port to the second LAG, and associate the remote switch identifier and the remote LAG identifier with the second LAG.

Abstract: A system and method of configuration of link aggregation groups includes a control unit and a port coupled to the control unit and configured to couple the network switching device to a neighboring switch. The control unit is configured to transmit a probe message to the neighboring switch, receive a remote switch identifier and link aggregation group (LAG) identifier from the neighboring switch, determine whether the remote switch identifier matches a previously received remote switch identifier and the remote LAG identifier matches a previously received remote LAG identifier. When both match, determine a first LAG associated with the previously received remote switch identifier and the previously received remote LAG identifier and assign the port to the first LAG. When both do not match, to create a second LAG, assign the port to the second LAG, and associate the remote switch identifier and the remote LAG identifier with the second LAG.

Abstract: A system and method of configuration of link aggregation groups includes a control unit and a port coupled to the control unit and configured to couple the network switching device to a neighboring switch. The control unit is configured to transmit a probe message to the neighboring switch, receive a remote switch identifier and link aggregation group (LAG) identifier from the neighboring switch, determine whether the remote switch identifier matches a previously received remote switch identifier and the remote LAG identifier matches a previously received remote LAG identifier. When both match, determine a first LAG associated with the previously received remote switch identifier and the previously received remote LAG identifier and assign the port to the first LAG. When both do not match, to create a second LAG, assign the port to the second LAG, and associate the remote switch identifier and the remote LAG identifier with the second LAG.

Abstract: The present invention relates to a process of obtaining recombinant lambdoid bacteriophage with high density display of functional peptides and proteins on surface of said phage comprising of: constructing a donor plasmid having a nucleotide sequence that defines the elements for replication of the vector in bacteria, a selectable marker, a nucleotide sequence flanked by two non-compatible recombination sequences, and an inducible cistron for expression of a capsid protein and a fusion protein; constructing a recipient phage having a nucleotide sequence that defines the lambdoid elements for replication and packaging of the vector into an assembled bacteriophage and encodes an inducible cistron for expression of a selectable marker flanked by two non-compatible recombination sequences; transferring the said donor plasmid to said recipient plasmid to obtain cointegrates; growing said cointegrates in selective liquid medium; harvesting phages displaying protein encoded by the foreign DNA encapsulated in said ha

Abstract: A semi-conducting material, a method for producing the material, and ways of implementing the material, wherein said material is doped with Cu or CuO, and is ferromagnetic at least at one temperature in the range between ?55° C. and 125° C. Typically the material may comprise GaP or GaN.

Abstract: A semi-conducting material being a non-oxide material or an already doped oxide material, wherein said material is doped with Manganese, Mn, and is ferromagnetic at least at one temperature in the range between room temperature and 500 K. Preferably, the Manganese doped material has a Manganese concentration at or below 5 at %.

Abstract: The present invention relates to a process of obtaining recombinant lambdoid bacteriophage with high density display of functional peptides and proteins on surface of said phage comprising of: constructing a donor plasmid having a nucleotide sequence that defines the elements for replication of the vector in bacteria, a selectable marker, a nucleotide sequence flanked by two non-compatible recombination sequences, and an inducible cistron for expression of a capsid protein and a fusion protein; constructing a recipient phage having a nucleotide sequence that defines the lambdoid elements for replication and packaging of the vector into an assembled bacteriophage and encodes an inducible cistron for expression of a selectable marker flanked by two non-compatible recombination sequences; transferring the said donor plasmid to said recipient plasmid to obtain cointegrates; growing said cointegrates in selective liquid medium; harvesting phages displaying protein encoded by the foreign DNA encapsulated in said ha