Mystick Womens Health 13 Bradlee Rd, Medford, MA 02155 7813951110 (phone)
Education:
Medical School Tufts University School of Medicine Graduated: 1985
Procedures:
Cesarean Section (C-Section) Colposcopy Delivery After Previous Caesarean Section Destruction of Benign/Premalignant Skin Lesions Destruction of Lesions on the Anus Hysterectomy Tubal Surgery Vaccine Administration Vaginal Delivery Vaginal Repair
Conditions:
Abnormal Vaginal Bleeding Breast Disorders Female Infertility Genital HPV Hemorrhoids
Languages:
English
Description:
Dr. Guthrie graduated from the Tufts University School of Medicine in 1985. She works in Medford, MA and specializes in Obstetrics & Gynecology. Dr. Guthrie is affiliated with Winchester Hospital.
Ellen Guthrie - Andover MA, US Theodore Davis - Boxford MA, US Jack Benner, II - South Hamilton MA, US
Assignee:
New England Biolabs, Inc. - Ipswich MA
International Classification:
C12Q 1/42 C12P 21/06 C12N 9/16
US Classification:
435 21, 435 681, 435196
Abstract:
Compositions for an alkaline phosphatase and methods for over-expression and purification of thermolabile Antarctic phosphatase (TAP) are provided. Uses for TAP include dephosphorylation of nucleic acids, sugars, peptides and proteins. TAP as described herein has advantages over phosphatases from other sources with respect to thermolability at 65 C. and efficiency of dephosphorylation activity at approximately neutral pH.
Dimitris Koutsioulis - Larissa, GR Ellen Guthrie - Andover MA, US
Assignee:
NEW ENGLAND BIOLABS, INC. - Ipswich MA
International Classification:
C12P 21/00 C12N 9/24 C07H 21/00
US Classification:
435 681, 435200, 536 232
Abstract:
Methods and compositions have been described that relate to a newly identified polypeptide family wherein each member has O-glycosidase activity and specified sequence characteristics. This family of enzymes can be used for example for cleaving O-linked glycans and for synthesis of neoglycopeptides or neoglycoproteins.
Method For Cloning And Producing The Naei Restriction Endonuclease And Methylase
Ellen P. Guthrie - Andover MA Elizabeth M. Van Cott - Malden MA Christopher H. Taron - Marblehead MA
Assignee:
New England Biolabs, Inc. - Beverly MA
International Classification:
C12N 922 C12N 1555
US Classification:
435199
Abstract:
The present invention is directed to a method for cloning and producing the NaeI restriction endonuclease by 1) introducing the restriction endonuclease gene from Nocardia aerocolonigenes into a host whereby the restriction gene is expressed; 2) fermenting the host which contains the plasmid encoding and expressing the NaeI restriction endonuclease activity, and 3) purifying the NaeI restriction endonuclease from the fermented host which contains the plasmid encoding and expressing the NaeI restriction endonuclease activity.
Isolated Dna Encoding The Sphi Restriction Endonuclease And Related Methods For Producing The Same
The present invention is directed to a method for cloning and producing the SphI restriction endonuclease by 1) introducing the restriction endonuclease gene from Streptomyces phaeochromogenes into a host whereby the restriction gene is expressed; 2) fermenting the host which contains the plasmid encoding and expressing the SphI restriction endonuclease activity, and 3) purifying the SphI restriction endonuclease from the fermented host which contains the plasmid encoding and expressing the SphI restriction endonuclease activity.
Method For Producing And Cloning Sacii Restriction Endonuclease And Methylase
Ellen P. Guthrie - Swampscott MA Marta M. Meda - Beverly MA
Assignee:
New England Biolabs, Inc. - Beverly MA
International Classification:
C12N 910 C12N 1554 C12N 1570 C12N 1576
US Classification:
435199
Abstract:
The present invention is directed to a method for cloning and producing the SacII restriction endonuclease by 1) introducing the restriction endonuclease gene from Streptomyces achromogenes into a host whereby the restriction gene is expressed; 2) fermenting the host which contains the plasmid encoding and expressing the SacII restriction endonuclease activity, and 3) purifying the SacII restriction endonuclease from the fermented host which contains the plasmid encoding and expressing the SacII restriction endonuclease activity.
Compositions and methods are provided for efficiently preparing a completely deglycosylated antibody where efficiency is measured in relative amounts of reagents in soluble or lyophilized form, and time and temperature of the reaction. Compositions and methods are also provided for separating substantially all N-linked glycans from a glycosylated antibody and for preserving functionality of the antibody. The methods are compatible with glycan labeling and protease digestion without the need for prior purification steps.
Compositions and methods are provided for efficiently preparing a completely deglycosylated antibody where efficiency is measured in relative amounts of reagents in soluble or lyophilized form, and time and temperature of the reaction. Compositions and methods are also provided for separating substantially all N-linked glycans from a glycosylated antibody and for preserving functionality of the antibody. The methods are compatible with glycan labeling and protease digestion without the need for prior purification steps.
Ellen Guthrie (1957-1960), Mary Garcia (1966-1970), John Smother (1969-1973), James Butler (1950-1952), Cecil McCleskey (1956-1960), Bill White (1962-1966)
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