Spore cheats addDNA why it doesn t work

It's normal, if you lose, you'll get the Harlequin Medal. Let's use modifiers, it's quick and easy.

I don't advocate using a cheat system though.

It is useful to press CTRL shirt C to open the console, then enter addDNA, and then press enter.

Some cheats can only be used in the device.

It is also possible that you will need to install the above patches before you can use it.

No cheats, only modifiers.

Well, of course, cheats will have a beneficial effect on you.

That's it.

There are two possibilities, 1. You don't get to the organism of the creature.

2. You have reached the tribe or stage above.

You can find 23 modifiers, which are better than cheats.

I have to enter it when installing components, and some of them just can't be used, and I often use moremoney

I need to input it when I install the component.

Yes, after you open the creature, press alt+shirt+c to enter, but you will be added a joker badge.

Yes, it must be entered in the creature creator to work.

Only uppercase can be entered in the cheat** console otherwise it will have no effect.

You have to modify the creature.

I need to input it when I install the component.

Because, when the card is up. A few more times will do.

(1) Mold spores were collected and diluted and coated in PDA medium labeled with cellophane, and fresh mycelium was collected after 20 h of incubation.

2) take g mycelium and place it in an ice-pre-cooled mortar, add g quartz sand and 2 ml of ice-pre-cooled ctab extract, add proteinase K to the final concentration of mg ml, and grind it on ice to form a homogeneous turbidity solution;

3) The liquid was transferred to a 5 ml centrifuge tube and 1 10 volumes of 10% SDS were added, and the liquid was cooled to room temperature after 65 warm baths for 20 30 min;

4) Add the same volume of Tris saturated phenol-chloroform (1:1) to extract twice, and transfer the upper aqueous phase to a new centrifuge tube;

5) Add the same volume of chloroform for extraction 1 time, and transfer the upper aqueous phase to a new centrifuge tube;

6) Add DNase-free RNAse A to a final concentration of 10 g mL and take a warm bath for 30 for 60 min.

7) Repeat step 5 once;

8) Add 2 times the volume of absolute ethanol to the upper aqueous phase and mix gently;

9) Gently pick out the chromosomal DNA with a sterile pipette nozzle, wash once in 70% ethanol, and cool dry the residual ethanol at room temperature;

10) Add an appropriate volume of TE solution to dissolve and store at 4.