青云翻译

Carrier pgapza multiple cloning sites in front of the constitutive expression of the gap promoter without inducer in the host bacteria gs1l5 can efficiently express foreign genes.

Vector pGAPZA multiple cloning sites before expression of GAP promoter, without inducing agent in host bacteria high expression of foreign genes in GS1l5.

In front of the carrier pGAPZA multi-clone position spot has the composition expression GAP start, does not need the derivative then in host fungus GS1l5 the highly effective expression extraneous source gene.

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Vector pGAPZA multiple cloning sites before expression of GAP promoter, without inducing agent in host bacteria high expression of foreign genes in GS1l5.