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K562红白血病细胞系中标记酶的分析:血红蛋白合成诱导时红细胞酶无协同表达。

Analysis of marker enzymes in the K562 erythroleukaemia cell line: no coordinate expression of red cell enzymes on induction of haemoglobin synthesis.

作者信息

Horton M A

出版信息

Biomed Pharmacother. 1982;36(4):213-6.

PMID:6819869
Abstract

Six sublines of the K562 erythroleukaemic cell line were examined by starch gel electrophoresis for the red cell enzymes carbonic anhydrase, CA I and II, pyruvate kinase, PK1 (R), and lactic dehydrogenase, LDH (B), both uninduced and following induction of haemoglobin synthesis with sodium butyrate or haemin. Neither CA or PK1 (R) enzymes were present constitutively found to be inducible characteristics; the LDH isoenzyme pattern showed equal expression of A and B subunits and did not change to the red cell form (B greater than A) on induction. Subline heterogeneity was also examined by analysis of a further 11 polymorphic enzymes, and cell line contamination was found not to account for the previously reported variations in inducibility by sodium butyrate.

摘要

通过淀粉凝胶电泳对K562红白血病细胞系的六个亚系进行了检测,以分析红细胞酶碳酸酐酶(CA I和II)、丙酮酸激酶(PK1 (R))和乳酸脱氢酶(LDH (B)),检测时细胞系未诱导,以及用丁酸钠或血红素诱导血红蛋白合成之后的情况。CA和PK1 (R)酶均未被发现有组成型表达,且具有可诱导特性;LDH同工酶模式显示A和B亚基表达相等,诱导后也未转变为红细胞形式(B大于A)。还通过分析另外11种多态性酶对亚系异质性进行了检测,发现细胞系污染并不能解释先前报道的丁酸钠诱导性的差异。

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