Compositions of highly-purified natural mixtures of type I Interferon derived from leukocytes and methods
    1.
    发明授权
    Compositions of highly-purified natural mixtures of type I Interferon derived from leukocytes and methods 失效
    来自白细胞的I型干扰素的高度纯化天然混合物的组合物和方法

    公开(公告)号:US06433144B1

    公开(公告)日:2002-08-13

    申请号:US09229039

    申请日:1999-01-12

    CPC classification number: C07K14/56 A61K38/00

    Abstract: This invention relates to methods for isolating highly purified mixtures of natural Type I interferon from white blood cells. The invention also relates to highly-purified mixtures of Type I interferon which resemble natural Type I interferon in that the highly purified mixtures of natural Type I interferon includes at least 9 subtypes, i.e., alpha-1, alpha-2, alpha-5, alpha-7, alpha-8, alpha-10, alpha-14, alpha-21 and omega, giving rise to at least 16, and possibly 20 or more molecular species, including alpha-1a, alpha-1new, alpha-2a, alpha-2b, alpha-2c, alpha-5, alpha-5LG, alpha-7, alpha-8a, alpha-8c, alpha-10a, alpha-14a, alphal4-b, alpha 14-c, alpha-14LG, alpha-21a, alpha-21b, alpha-21c, omega and omega LG.

    Abstract translation: 本发明涉及从白细胞中分离出高度纯化的天然I型干扰素混合物的方法。 本发明还涉及类似于天然I型干扰素的I型干扰素的高度纯化的混合物,因为天然I型干扰素的高度纯化的混合物包括至少9种亚型,即α-1,α-2,α-5, α-7,α-8,α-10,α-14,α-21和ω,产生至少16种,并且可能有20种或更多种分子物质,包括α-1a,α-1新,α-2a, α-2b,α-2c,α-5,α-5LG,α-7,α-8a,α-8c,α-10a,α-14a,alphal4-b,α14-c,α-14LG, -21a,α-21b,α-21c,ω和ωLG。

    Method for labeling DNA by ring-opening of purine bases
    2.
    发明授权
    Method for labeling DNA by ring-opening of purine bases 失效
    通过嘌呤碱基开环标记DNA的方法

    公开(公告)号:US5593829A

    公开(公告)日:1997-01-14

    申请号:US241385

    申请日:1994-05-03

    Applicant: Mead M. McCabe

    Inventor: Mead M. McCabe

    Abstract: The invention provides methods for attaching detectable labels to the N.sup.7 -formyl group, of imidazole ring-opened alkylated purines and purine derivatives, directly, through a linking group, or by subsequent derivatization of a blocking group. The invention provides simple and efficient methods for labeling polynucleotides. In addition, the invention provides derivatized ring-opened alkylated purines and purine derivatives, including reagents for chemical and enzymatic synthesis of detectably labeled polynucleotides.

    Abstract translation: 本发明提供了通过连接基团直接将可检测标记连接到咪唑开环烷基化嘌呤和嘌呤衍生物的N7-甲酰基,咪唑开环烷基化嘌呤和嘌呤衍生物的方法,或通过随后的封闭基团的衍生化。 本发明提供用于标记多核苷酸的简单而有效的方法。 此外,本发明提供衍生化的开环烷基化嘌呤和嘌呤衍生物,包括用于化学和酶合成可检测标记的多核苷酸的试剂。

    Ring-opened purine compounds for labeling polynucleotides
    3.
    发明授权
    Ring-opened purine compounds for labeling polynucleotides 失效
    用于标记多核苷酸的开环嘌呤化合物

    公开(公告)号:US5656742A

    公开(公告)日:1997-08-12

    申请号:US469925

    申请日:1995-06-06

    Applicant: Mead M. McCabe

    Inventor: Mead M. McCabe

    Abstract: The invention provides methods for attaching detectable labels to the N.sup.7 -formyl group, of imidazole ring-opened alkylated purines and purine derivatives, directly, through a linking group, or by subsequent derivatization of a blocking group. The invention provides simple and efficient methods for labeling polynucleotides. In addition, the invention provides derivatized ring-opened alkylated purines and purine derivatives, including reagents for chemical and enzymatic synthesis of detectably labeled polynucleotides.

    Abstract translation: 本发明提供了通过连接基团直接将可检测标记连接到咪唑开环烷基化嘌呤和嘌呤衍生物的N7-甲酰基,咪唑开环烷基化嘌呤和嘌呤衍生物的方法,或通过随后的封闭基团的衍生化。 本发明提供用于标记多核苷酸的简单而有效的方法。 此外,本发明提供衍生化的开环烷基化嘌呤和嘌呤衍生物,包括用于化学和酶合成可检测标记的多核苷酸的试剂。

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