Application
The anti-CKM Pab is used in Western blot to detect CKM in mouse heart tissue lysate.Application
Western blot analysis of CKM (arrow) using rabbit polyclonal CKM-T6 . 293 cell lysates (2 ug/lane) either nontransfected (Lane 1) or transiently transfected (Lane 2) with the CKM gene.| Product Name | CKM Antibody (N-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | CKM; CKMM; Creatine kinase M-type; Creatine kinase M chain; M-CK |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WB |
| WB:1:100~500 |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | CKMM |
|---|---|
| Alternative Names | CKM CKMM Creatine kinase M-type Creatine kinase M chain M-CK |
| Molecular Weight(MW) | 43101 Da |
| Function | Reversibly catalyzes the transfer of phosphate between ATP and various phosphogens (e.g. creatine phosphate). Creatine kinase isoenzymes play a central role in energy transduction in tissues with large, fluctuating energy demands, such as skeletal muscle, heart, brain and spermatozoa |
| Tissue Specificity | This CKM Antibody antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1~30 amino acids from the N-terminal region of human CKM. |
| Cellular Localization | Cytoplasm. |
| Entrez Gene | 1158 |
|---|
Application
The anti-CKM Pab is used in Western blot to detect CKM in mouse heart tissue lysate.
Application
Western blot analysis of CKM (arrow) using rabbit polyclonal CKM-T6 . 293 cell lysates (2 ug/lane) either nontransfected (Lane 1) or transiently transfected (Lane 2) with the CKM gene.| Application Notes | WB:1:100~500 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles. |
| Storage Buffer | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS. |
