Technical supportFrontier Communication DeLand, FL Aug 2009 to Jan 2010 Customer Service RepresentativeMetavante Madison, WI Nov 2007 to Aug 2008 Customer Service Representative
Skills:
More than 8 years successful experience in customer service and support with recognized strengths in problem-solving and trouble-shooting. Possess solid computer skills. Excellent working knowledge using both Windows and Mac systems; All Microsoft software, HTML, Java and C ++ A team player, acknowledged as Total Quality Customer Service Professional. Extremely productive in a high volume, high stress, environment.
Sierra Orthopedics 1780 E Florence Blvd STE 106, Casa Grande, AZ 85122 5208368988 (phone), 5208367930 (fax)
Education:
Medical School University of Illinois, Chicago College of Medicine Graduated: 1979
Procedures:
Arthrocentesis Carpal Tunnel Decompression Hip Replacement Knee Arthroscopy Knee Replacement Shoulder Arthroscopy Hip/Femur Fractures and Dislocations Lower Arm/Elbow/Wrist Fractures and Dislocations Lower Leg/Ankle Fractures and Dislocations Shoulder Surgery
Conditions:
Fractures, Dislocations, Derangement, and Sprains Internal Derangement of Knee Internal Derangement of Knee Cartilage Internal Derangement of Knee Ligaments Intervertebral Disc Degeneration
Languages:
English Spanish
Description:
Dr. Erickson graduated from the University of Illinois, Chicago College of Medicine in 1979. He works in Casa Grande, AZ and specializes in Orthopaedic Surgery and Orthopedic Sports Medicine. Dr. Erickson is affiliated with Banner Casa Grande Medical Center.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
A cyanine dye having the formula wherein R -R are each independently selected from a group consisting of hydrogen, C -C alkyl group, and C -C alkyl group having a hydrophilic substituent thereon. R and R are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA Joseph John Miller - Dracut MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
Assignee:
NEN Life Science Products, Inc. - Boston MA
International Classification:
C07D27904 C07D41704 C07D27762 C07D27760 C07D26352
US Classification:
548152
Abstract:
A cyanine dye having the formula ##STR1## wherein R. sub. 1 --R. sub. 8 are each independently selected from a group consisting of hydrogen, C. sub. 1 -C. sub. 6 alkyl group, and C. sub. 0 -C. sub. 4 alkyl group having a hydrophilic substituent thereon. R. sub. 11 and R. sub. 12 are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
Compounds And Method For Synthesizing Sulfoindocyanine Dyes
Mark Norman Bobrow - Lexington MA Thomas Joseph Erickson - Carlisle MA
Assignee:
E. I. Du Pont de Nemours and Company - Wilmington DE
International Classification:
C07D40306
US Classification:
548455
Abstract:
Novel intermediates having an indolenine nucleus which are useful in the synthesis of fluorescent sulfoindocyanine dyes are described. Dyes synthesized using such intermediates do not contain a reactive group that will covalently attach to a target molecule at an amine- or hydroxy-containing site. Rather, these intermediates are linked to an enzyme substrate or a member of a specific binding pair. Also included are tyramide-comaining sulfonidocyanine dyes.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA Joseph John Miller - Dracut MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
A cyanine dye having the formula ##STR1## wherein R. sub. 1 -R. sub. 8 are each independently selected from a group consisting of hydrogen, C. sub. 1 -C. sub. 6 alkyl group, and C. sub. 0 -C. sub. 4 alkyl group having a hydrophilic substituent thereon. R. sub. 11 and R. sub. 12 are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA Joseph John Miller - Dracut MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
Assignee:
NEN Life Science Products, Inc. - Boston MA
International Classification:
C07D27916 C07D24136 C07D41704 C07D27760 C07D40302
US Classification:
544 51
Abstract:
A cyanine dye having the formula ##STR1## wherein R. sub. 1 -R. sub. 8 are each independently selected from a group consisting of hydrogen, C. sub. 1 -C. sub. 6 alkyl group, and C. sub. 0 -C. sub. 4 alkyl group having a hydrophilic substituent thereon. R. sub. 11 and R. sub. 12 are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.
Compounds And Method For Synthesizing Sulfoindocyanine Dyes
Mark Norman Bobrow - Lexington MA Thomas Joseph Erickson - Carlisle MA
Assignee:
E. I. du Pont de Nemours and Company - Wilmington DE
International Classification:
C07D20908
US Classification:
548455
Abstract:
Novel intermediates having an indolenine nucleus which are useful in the synthesis of fluorescent sulfoindocyanine dyes are described. Dyes synthesized using such intermediates do not contain a reactive group that will covalently attach to a target molecule at an amine- or hydroxy-containing site. Rather, these intermediates are linked to an enzyme substrate or a member of a specific binding pair. Also included are tyramide-containing sulfonidocyanine dyes.
Malcolm Harry Randall - Wayland MA Philip Richard Buzby - Brockton MA Thomas Joseph Erickson - Carlisle MA Joseph David Trometer - Framingham MA Joseph John Miller - Dracut MA David George Ahern - Lexington MA Mark Norman Bobrow - Lexington MA
Assignee:
NEN Life Science Products, Inc. - Boston MA
International Classification:
C07D27904 C07D41704 C07D27762 C07D27760 C07D26352
US Classification:
48152
Abstract:
A cyanine dye having the formula ##STR1## wherein R. sub. 1 -R. sub. 8 are each independently selected from a group consisting of hydrogen, C. sub. 1 -C. sub. 6 alkyl group, and C. sub. 0 -C. sub. 4 alkyl group having a hydrophilic substituent thereon. R. sub. 11 and R. sub. 12 are chosen to include a free or protected thiol, amine or hydroxyl substituent capable of reacting with a target molecule through a nucleophilic displacement mechanism. The dye is useful in labeling a variety of target molecules. Processes are described for synthesizing suitable heterocyclic and indole derivatives as precursors for the aforementioned cyanine dyes.