KR900018379A - 암전이 억제인자의 제조방법 - Google Patents

암전이 억제인자의 제조방법 Download PDF

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KR900018379A
KR900018379A KR1019900007373A KR900007373A KR900018379A KR 900018379 A KR900018379 A KR 900018379A KR 1019900007373 A KR1019900007373 A KR 1019900007373A KR 900007373 A KR900007373 A KR 900007373A KR 900018379 A KR900018379 A KR 900018379A
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cancer metastasis
cells
warm
blooded animal
producing
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KR0157227B1 (ko
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마사시 구리모도
류유이찌 모도다
간소오 이와끼
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하야시바라 겐
가부시기가이샤 하야시바라 세이부쓰 가가구겡규우죠
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Abstract

내용 없음

Description

암전이 억제인자의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (11)

  1. 암전이 억제인자 산생능을 지닌 배양주화된 인체조혈기관으로 연유하는 세포를 이용하여 암전이 억제인자를 산생시켜 이것을 채취하는 것을 특징으로 하는 암전이억제인자의 제조방법.
  2. 제1항에 있어서, 인체조형기관으로 연유하는 세포가 인체이외의 온혈동물체내에 이식되고, 그 온혈동물을 기르는 과정에서 그 온형동물의 채액을 받으면서 증식하여 얻을 수 있는 세포임을 특징으로 하는 암전이억제인자의 제조방법.
  3. 제2항에 있어서, 인체이외의 온혈동물이 새 또는 포유동물인 것을 특징으로 하는 암전이억제인자의 제조방법.
  4. 제1항에 있어서, 인체조혈기관으로 연유하는 세포가, 인체이외의 온혈동물체내 그렇지 않으며 체외에 부착한 확산챔버내애 이식되고, 그 온혈동물을 기르는 과정에서 그 온혈동물의 체액을 받으면서 증식하여 얻을수 있는 세포임을 특징으로 하는 암전이억제인자의 제조방법.
  5. 제4항에 있어서, 상기 인체이외의 온혈동물이 새 또는 포유동물인 것을 특징으로 하는 암전이억제인자의 제조방법.
  6. 제1항에 있어서, 인체조혈기관으로 연유하는 세포가 T-세포임을 특징으로 하는 암전이억제인자의 제조방법.
  7. 제1항에 있어서, 암전이억제인자의 산생에 있어, 암전이 억제인자산생능을 지닌 배양주화된 인체조혈기로 연유하는 세포에 유도제를 접촉시키는 것을 특징으로 하는 암전이억제인자의 제조방법.
  8. 제7항에 있어서, 암전이억제인자 유도제가 미토겐임을 특징으로 하는 암전이억제인지의 제조방법.
  9. 제1항에 있어서, 암전이억제인자가, 인체대장암으로 연유하는 배양주화된 세포 RPMI 4788(미생물 공업 연구소 조례기생충 제2429호)으로 분석되었을 때 전이억제활성을 나타내고, 인터페론활성, 종양괴상인자활성, 인터로이킨 1활성 및 인터로이킨 2활성을 나타내지 않고, 겔여과법에서 분자량 10,000-45,000의 범위에 있는 물질임을 특징으로 하는 암전이 억제인자의 제조방법.
  10. 제1항에 있어서, 배양주화된 인체조혈기관으로 연유하는 세포가 RAMOS 세포(ATCC CRL 1596) HPB-MLT 세포(FERM BP-2430), MOLT-3세포(ATCC CRL 1552), TALL-1 세포(JCRB 0086) 및 U-937 세포 (ATCC CRL 1593)로 구성된 그룹에서 선택된 것임을 특징으로 하는 암전이억제인자의 제조방법.
  11. 제1항의 방법에 의하여 향상 제조되는 암전이억제인자.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019900007373A 1989-05-22 1990-05-22 암 전이 억제인자의 제조방법 KR0157227B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP1-128362 1989-05-22
JP1128362A JP2926409B2 (ja) 1989-05-22 1989-05-22 癌転移抑制因子の製造方法
JP89-128362 1989-05-22

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KR900018379A true KR900018379A (ko) 1990-12-21
KR0157227B1 KR0157227B1 (ko) 1998-10-15

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US (1) US5126148A (ko)
EP (1) EP0401997B1 (ko)
JP (1) JP2926409B2 (ko)
KR (1) KR0157227B1 (ko)
AT (1) ATE127527T1 (ko)
CA (1) CA2017279A1 (ko)
DE (1) DE69022121T2 (ko)
DK (1) DK0401997T3 (ko)
ES (1) ES2080114T3 (ko)
GR (1) GR3018004T3 (ko)
RU (1) RU2070046C1 (ko)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3439490B2 (ja) * 1992-09-28 2003-08-25 株式会社林原生物化学研究所 蛋白質とその蛋白質をコードするdna並びにその蛋白質の製造方法
JPH1080270A (ja) * 1996-07-19 1998-03-31 Hayashibara Biochem Lab Inc ポリペプチドをプロセッシングする酵素

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4785077A (en) * 1986-05-05 1988-11-15 Scripps Clinic And Research Foundation Substantially pure cytotoxicity triggering factor

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Publication number Publication date
EP0401997A1 (en) 1990-12-12
DE69022121D1 (de) 1995-10-12
US5126148A (en) 1992-06-30
GR3018004T3 (en) 1996-02-29
KR0157227B1 (ko) 1998-10-15
DK0401997T3 (da) 1995-10-16
RU2070046C1 (ru) 1996-12-10
JP2926409B2 (ja) 1999-07-28
DE69022121T2 (de) 1996-04-04
JPH02308799A (ja) 1990-12-21
CA2017279A1 (en) 1990-11-22
EP0401997B1 (en) 1995-09-06
ES2080114T3 (es) 1996-02-01
ATE127527T1 (de) 1995-09-15

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