You Searched For: James+Walker+Ireland+Ltd

Catalog Number: (89174-704)

Supplier: Hamilton

Description: Microlab® 600 UK, Ireland, Malaysia, Middle East Power Cord

Catalog Number: (76192-384)

Supplier: Sklar

Description: The Sklar® TC Thomson-Walker Bozeman needle holder is a ratched finger ring instrument to hold curved needles while suturing.

Catalog Number: (470002-352)

Supplier: John Wiley & Sons

Description: Pam Walker and Elaine Wood

Catalog Number: (103633-102)

Supplier: Sino Biological

Description: A DNA sequence encoding the Influenza A virus (A/turkey/Ireland/1378/1983(H5N8)) hemagglutinin (P11135) (Met1-Arg339), termed as HA1, was expressed with a polyhistidine tag at the C-terminus.

Catalog Number: (103633-100)

Supplier: Sino Biological

Description: A DNA sequence encoding the Influenza A virus (A/turkey/Ireland/1378/1983(H5N8)) hemagglutinin (ABI85117.1) (Met1-Gln527), termed as HA, was expressed with a polyhistidine tag at the C-terminus.

Catalog Number: (76101-436)

Supplier: Bioss

Description: Acts as component of the MCM2-7 complex (MCM complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity. Required for the entry in S phase and for cell division.

Catalog Number: (76011-874)

Supplier: Prosci

Description: The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.

Catalog Number: (470007-256)

Supplier: KELLER BROS. & MILLER, INC.

Description: Developed by Teacher James Ross, the Core-Valence-Radius Periodic Table is a new type of periodic table designed to make learning chemistry a more intuitive process. Each element is represented by a nucleus (core), a valence shell, and an electronegativity value.

Catalog Number: (10351-994)

Supplier: Bioss

Description: Acts as component of the MCM2-7 complex (MCM complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity (By similarity). Interacts with MCMBP.

Catalog Number: (10351-990)

Supplier: Bioss

Description: Acts as component of the MCM2-7 complex (MCM complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity (By similarity). Interacts with MCMBP.

Catalog Number: (10751-352)

Supplier: Prosci

Description: ATAD3A Antibody: ATAD3A is a member of the AAA ATPase family, a family of proteins that catalyze ATP into ADP and are involved in several cellular functions such as cell-cycle regulation, protein proteolysis and transport. The AAA ATPase family is characterized by a highly conserved AAA motif containing Walker homology sequences and imparting ATPase activity. Mitochondrial membrane proteins ATAD3A/B contribute to the stabilization of nucleoids and may participate in the transformation pathway and the chemosensitivity of oligodendrogliomas. The gene encoding ATAD3A/B/C maps to human chromosome 1 and has been suggested to be an anti-apoptotic marker.

Catalog Number: (470002-358)

Supplier: Kemtec

Description: James Sutton

Catalog Number: (470022-966)

Supplier: FELINE PRESS

Description: James L. Castner

Supplier: Elkay Plastics

Description: Elkay has a full range of DME equipment covers available for all types of accreditation purposes

Catalog Number: (10427-254)

Supplier: Bioss

Description: POMT1 (Protein O mannosyl transferase 1) is a multipass membrane protein that is found in the endoplasmic reticulum. POMT1 catalyses the transfer of mannosyl residues to the hydroxyl groups of serine or threonine residues. Enzymatic activity is dependent on co expression of POMT1 with POMT2. Defects in the POMT1 gene are associated with Walker-Warburg syndrome (WWS), a congential muscular dystrophy that is associated with mental retardation and is usually lethal within the first few months of life. Other defects in the POMT1 gene result in limb girdle muscular dystrophy type 2K (LGMD2K), which is associated with mild mental retardation. Studies in Drosophila suggest that mutation of POMT1 alters the efficacy of synaptic transmission and a change in subunit composition of post synaptic glutamate receptors at the neuromuscular junction. Missense mutations in POMT1 have been associated with glioneuronal and glial brain tumours.

Catalog Number: (10427-268)

Supplier: Bioss

Description: POMT1 (Protein O mannosyl transferase 1) is a multipass membrane protein that is found in the endoplasmic reticulum. POMT1 catalyses the transfer of mannosyl residues to the hydroxyl groups of serine or threonine residues. Enzymatic activity is dependent on co expression of POMT1 with POMT2. Defects in the POMT1 gene are associated with Walker-Warburg syndrome (WWS), a congential muscular dystrophy that is associated with mental retardation and is usually lethal within the first few months of life. Other defects in the POMT1 gene result in limb girdle muscular dystrophy type 2K (LGMD2K), which is associated with mild mental retardation. Studies in Drosophila suggest that mutation of POMT1 alters the efficacy of synaptic transmission and a change in subunit composition of post synaptic glutamate receptors at the neuromuscular junction. Missense mutations in POMT1 have been associated with glioneuronal and glial brain tumours.