MAKE UP PRIMER

Brand Owner (click to sort) Address Description
DEZONE Hangzhou Jin Cai Cosmetics Co., Ltd. ROOM 1606 Huanyu Buliding, NO626Science Museum St Hangzhou 310051 China Make-up primer; Chalk for make-up; Eye make-up remover; Eyes make-up; Facial make-up;
EGLRI JEONG, BANGHUI 1 dong 25, Oseong 1-gil, Seobuk-gu Cheonan,Chungcheonamdo 31090 Republic of Korea make-up primer; glue removers; eyelash extension glue in the nature of adhesives for attaching eyelash extensions; cosmetics, namely, protein remover in the nature of eyelash primer; false nails made of powder and liquid acrylics; false nails made of polymer resin;The wording EGLRI has no meaning in a foreign language.;
HYDRO MAGNET L'OREAL USA CREATIVE, INC. 10 Hudson Yards New York NY 10001 Make-up primer;
PRIME COLLAGEN Dew Beauty Inc. 15945 10th Concession Schomberg, Ontario L0G1T0 Canada Make-up primer; Facial make-up, namely, facial primer in the nature of a moisturizing cream; all of the foregoing containing collagen;COLLAGEN;
SUEDE SUNRISE Summer Fridays 10345 W. Olympic Blvd., Suite 102 Los Angeles CA 90064 make-up primer; cosmetic sunscreen preparations;
 

Where the owner name is not linked, that owner no longer owns the brand

    
Technical Examples
  1. The present invention provides methods for detecting and identifying sequence variations in a nucleic acid sequence of interest using a detector primer. It has been found that the reduced efficiency of primer extension by DNA polymerases when the 3' end of a primer does not hybridize perfectly with the target can be adapted for use as a means for distinguishing or identifying the nucleotide in the target which is at the site where the diagnostic mismatch between the detector primer and the target occurs. The detector primer hybridizes to the sequence of interest and is extended with polymerase. The efficiency of detector primer extension is detected as an indication of the presence and/or identity of the sequence variation in the target. The inventive methods make use of nucleotide mismatches at or near the 3' end of the detector primer to discriminate between the nucleotide sequence of interest and a second nucleotide sequence which may occur at that same site in the target. The methods are particularly well suited for detecting and identifying single nucleotide differences between a target sequence of interest (e.g., a mutant allele of a gene) and a second nucleic acid sequence (e.g., a wild type allele for the same gene).