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Calcite | Level 5

Hi all, 


I have a confusion selecting right statistical method to analyse my data (please see the attached excel file as an example). 


I have used 4 different extraction method (EM_1 to EM_4) to release protein from bacteria. But I have used 2 methods to determine the amount of protein release from these 4 different extraction techniques. I am interested in comparing the efficiency of 4 extraction methods as well as comparing the amount of protein obtained in two different conditions (that is in cell solution and cell-free solution). Basically, my independent variables/treatments are 4 extraction methods and my outcome (dependent variable) is amount of protein release from each extraction method. However, I am also interested in  showing amount of protein  in two conditions (that is protein amount in cell solution and cell-free solution). So, these two conditions , though are outcome (dependent variables) seems like treatment,  because I want to compare and say protein is higher /lower in one of these conditions. 


My question;

1. Is this one way ANOVA ? 

2. Is this 2 way anova (Completely randomized design)

3. Is this 2 way ANOVA (completely randomized block design , two conditions of protein amount as a block)


Please suggest me what type of analysis is suitable for these data set ? 


Thank you very much ! 


Rhodochrosite | Level 12 sld
Rhodochrosite | Level 12

I would say that your treatment structure is a two-way factorial: extraction method (4 levels) and condition (2 levels). But you have not told us anything about your design structure so we have no way of knowing whether the design is a CRD, or a RCBD, or a split-plot, etc.


If you do an internet search on "experiment treatment structure design structure", you'll find several helpful links.


I hope this helps.


Calcite | Level 5
Thank you so much for your reply.

My design is RCBD. My two conditions are block and each block contains all
treatments that is extraction methods (EM_1 to EM_4). I want to make two
conditions (protein in solution and protein in cell-free solution) as a
block. Since, these two conditions are the sources of variations that are
not related to the treatments.

I tried to right code for this analysis but could not succeed. I have only
done one way anova using SAS earlier, and now I am having difficulties
analyzing data. would you please help me writing a code for the data

*data* enzyme;

input ext_methods;

do block = *1* to *? (could not figured out what should i write here)*

input protein ;




could not figured out how I place data here.


*proc* *glm*;

class block ? ;

model protein=block ? ;
*run*; *quit*

Rhodochrosite | Level 12 sld
Rhodochrosite | Level 12

I regret that I am not able to figure out your design structure from the additional information that you've provided.


I doubt that two blocks are defined by the two conditions. Blocks are typically considered to be random effects factors which determine the variance of the response and do not affect the mean of the response. I believe you are thinking of condition as a fixed effects factor; if condition is a fixed effects factor, then it cannot also be a random effects factor. So you'll want to think more about your design structure.


Blocks are clusters of experimental units: units within a particular block are assumed to be "similar", and units between blocks are assumed to be "different". You may have clustering in your experimental design, or you may not.


Design issues can be complicated, so if there is someone at your institution who could help, I suggest talking with them. There is, of course, a lot of books, papers, etc. on the topic of design.


Or you could try again here, with a lot more detail about how you ran the experiment. 


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