Abstract: A method for testing a serial over local area network (SOL) function of a motherboard of a computing device. The method determines that the SOL function is normal if forward data can be transmitted from the serial port of the motherboard to a network interface controller (NIC) of the motherboard through a predefined path, and backward data can be transmitted from the NIC to the serial port through a predefined reverse path. The method determines that the SOL function is abnormal if the forward data cannot be transmitted from the serial port to the NIC through the predefined path, or the backward data cannot be transmitted from the NIC to the serial port through the predefined reverse path.

Abstract: Disclosed are charging control methods for a rechargeable battery and portable computers. The charging control method includes acquiring a control parameter for a charge current of the rechargeable battery; modifying, based on the control parameter, the charge current from a first charge current to a second charge current less than the first charge current; and charging the rechargeable battery with the second charge current. Compared with conventional methods of charging the battery always with the maximal charge current, the present disclosure can improve the battery's lifetime.

Abstract: The present invention provides a battery management device and a portable computer, the battery management device is for managing the rechargeable battery provided in a portable computer, the portable computer is provided with a charge circuit for charging a battery, the battery management device comprises: a discharge circuit for discharge the battery; a acquiring module for acquire the mode determining parameter; a first determining module for judging whether the battery storage mode is entered according to the mode determining parameter; a first control module for controlling the charge circuit or the discharge circuit to control the amount of electrical charge of the battery so that the amount of electrical charge of the battery is lower than the second amount of electrical charge threshold in the battery storage mode; the performance of the battery when deposited with the amount of electrical charge lower than the second amount of electrical charge threshold is better than the performance when deposited

Abstract: The present invention provides a method of determining the optimal composition of a serum-free, eukaryotic cell culture medium supplement, using 2-level factorial design and the steepest ascent method. The invention further provides a method of making a serum-free eukaryotic cell culture medium supplement and the generated thereof. The invention further provides a method of making a serum-free, eukaryotic cell culture medium and the medium generated thereof. The invention further provides a kit containing the medium of the invention. The invention also provides a method of expanding CD34<+> hematopoietic cells and a composition comprising CD34<+> hematopoietic cells in a serum-free, eukaryotic cell culture medium of the invention.

Abstract: Controlling methods for handheld devices with a touch display unit are provided. The controlling method includes the steps of: detecting a sliding gesture on the touch display unit when the handheld device is locked; in response to the detected sliding gesture, displaying at least one indication data on the touch display unit, wherein the indication data includes an indication object and the indication object rotates/flips around a central axis of the touch display unit and a rotating/flipping status of the indication object indicates an unlocking status in response to a detected contact position corresponding to the sliding gesture; and determining whether to unlock the handheld device according to the rotating/flipping status of the indication object.

Abstract: A sequential solid phase immunoassay and system is disclosed. The immunoassay utilizes the secondary antibody method for the detection of antibodies in a membrane-based test. The system comprises a test strip including a nitrocellulose membrane having an immobilized antigen in a capture zone on the membrane and a stabilized liquid secondary antibody conjugate. The sequential solid phase immunoassay is performed in a sequential manner with the addition of a fluid specimen being followed by the addition of the stabilized liquid secondary antibody conjugate. The sequential procedure using the system includes allowing the fluid specimen containing antibodies specific to the antigen to pass laterally from the test strip first end through the capture zone. The immobilized antigens in the capture zone capture antibodies specific to the antigen. The stabilized liquid secondary antibody conjugate then binds to the captured antibodies and can be detected visually or by a machine or reader.

Abstract: Disclosed are charging control methods for a rechargeable battery and portable computers. The charging control method includes acquiring a control parameter for a charge current of the rechargeable battery; modifying, based on the control parameter, the charge current from a first charge current to a second charge current less than the first charge current; and charging the rechargeable battery with the second charge current. Compared with conventional methods of charging the battery always with the maximal charge current, the present disclosure can improve the battery's lifetime.

Abstract: A power adapter for a portable computer includes a pulse width modulation unit and an output shaping unit and further includes a first judgment module that judges whether the portable computer is in a first state according to state judging parameters, and compares an output voltage with a first preset voltage and a second preset voltage when judging that the portable computer is in the first state, and acquires a judging result, wherein the first preset voltage is greater than or equal to the second preset voltage. The power adapter can increase efficiency.

Abstract: The present invention relates to the manipulations of expression levels or enzymatic activities of PRMTs differentially regulate hematopoietic differentiation toward megakaryocytes or erythrocytes. The modulation of lineage fates of megakaryocyte-erythrocyte progenitors is useful for various purposes, including particular regulation of hematopoiesis for therapy and manufacture of individual blood cells for transplantation.

Abstract: The present invention provides a battery management device and a portable computer, the battery management device is for managing the rechargeable battery provided in a portable computer, the portable computer is provided with a charge circuit for charging a battery, the battery management device comprises: a discharge circuit for discharge the battery; a acquiring module for acquire the mode determining parameter; a first determining module for judging whether the battery storage mode is entered according to the mode determining parameter; a first control module for controlling the charge circuit or the discharge circuit to control the amount of electrical charge of the battery so that the amount of electrical charge of the battery is lower than the second amount of electrical charge threshold in the battery storage mode; the performance of the battery when deposited with the amount of electrical charge lower than the second amount of electrical charge threshold is better than the performance when deposited

Abstract: The present invention provides a method of determining the optimal composition of a serum-free, eukaryotic cell culture medium supplement, using 2-level factorial design and the steepest ascent method. The invention further provides a method of making a serum-free eukaryotic cell culture medium supplement and the generated thereof. The invention further provides a method of making a serum-free, eukaryotic cell culture medium and the medium generated thereof. The invention further provides a kit containing the medium of the invention. The invention also provides a method of expanding CD34<+> hematopoietic cells and a composition comprising CD34<+> hematopoietic cells in a serum-free, eukaryotic cell culture medium of the invention.

Abstract: Disclosed herein are media and processes for the ex vivo production of megakaryocytes from human CD34+ cells, in which human CD34+ cells, either being freshly isolated from a newborn's cord blood or having been subcultured in an expansion medium after isolation from a newborn's cord blood, are subjected to cultivation in a cultivating medium consisting essentially of a basal medium, a serum substitute and a cytokine cocktail, wherein the serum substitute consists of human serum albumin, insulin, and transferrin; and the cytokine cocktail consists of thrombopoietin (TPO), stem cell factor (SCF), Flt-3 ligand (FL), interleukin-3 (IL-3), IL-6, IL-9, and granulocyte-macrophage colony-stimulating factor (GM-CSF).

Abstract: A sequential solid phase immunoassay and system is disclosed. The immunoassay utilizes the secondary antibody method for the detection of antibodies in a membrane-based test. The system comprises a test strip including a nitrocellulose membrane having an immobilized antigen in a capture zone on the membrane and a stabilized liquid secondary antibody conjugate. The sequential solid phase immunoassay is performed in a sequential manner with the addition of a fluid specimen being followed by the addition of the stabilized liquid secondary antibody conjugate. The sequential procedure using the system includes allowing the fluid specimen containing antibodies specific to the antigen to pass laterally from the test strip first end through the capture zone. The immobilized antigens in the capture zone capture antibodies specific to the antigen. The stabilized liquid secondary antibody conjugate then binds to the captured antibodies and can be detected visually or by a machine or reader.

Abstract: A stroma-free, serum-free, and chemically defined medium and a method for mononuclear cell expansion ex vivo using the same. An exemplary medium includes a basal medium, a serum substitute, and a cytokine formula.

Abstract: The present invention provides a method of determining the optimal composition of a serum-free, eukaryotic cell culture medium supplement, using 2-level factorial design and the deepest ascent method. The invention further provides a method of making a serum-free eukaryotic cell culture medium supplement and the generated thereof. The invention further provides a method of making a serum-free, eukaryotic cell culture medium and the medium generated thereof. The invention further provides a kit containing the medium of the invention. The invention also provides a method of expanding CD34<+> hematopoietic cells and a composition comprising CD34<+> hematopoietic cells in a serum-free, eukaryotic cell culture medium of the invention.

Abstract: A stroma-free, serum-free, and chemically defined medium and a method for mononuclear cell expansion ex vivo using the same. An exemplary medium includes a basal medium, a serum substitute, and a cytokine formula.

Abstract: A stroma-free, serum-free, and chemically defined medium and a method for mononuclear cell expansion ex vivo using the same. An exemplary medium includes a basal medium, a serum substitute, and a cytokine formula.

Abstract: The present invention provides a method of determining the optimal composition of a serum-free, eukaryotic cell culture medium supplement, using 2-level factorial design and the deepest ascent method. The invention further provides a method of making a serum-free eukaryotic cell culture medium supplement and the generated thereof. The invention further provides a method of making a serum-free, eukaryotic cell culture medium and the medium generated thereof. The invention further provides a kit containing the medium of the invention. The invention also provides a method of expanding CD34<+> hematopoietic cells and a composition comprising CD34<+> hematopoietic cells in a serum-free, eukaryotic cell culture medium of the invention.