Application
Western blot analysis of SCRN3 Antibody (C-term) in K562 cell line lysates (35ug/lane). SCRN3 (arrow) was detected using the purified Pab.Application
Western blot analysis of SCRN3 Antibody (C-term) in mouse cerebellum tissue lysates (35ug/lane). SCRN3 (arrow) was detected using the purified Pab.Application
SCRN3 Antibody (C-term) flow cytometric analysis of K562 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.| Product Name | SCRN3 Antibody (C-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | SCRN3; Secernin-3 |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WBFC |
| WB:1:100~500 FC |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Alternative Names | SCRN3 Secernin-3 |
|---|---|
| Molecular Weight(MW) | 48544 Da |
| Tissue Specificity | This SCRN3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between amino acids 330-360 from the C-terminal region of human SCRN3. |
| Entrez Gene | 79634 |
|---|
Application
Western blot analysis of SCRN3 Antibody (C-term) in K562 cell line lysates (35ug/lane). SCRN3 (arrow) was detected using the purified Pab.
Application
Western blot analysis of SCRN3 Antibody (C-term) in mouse cerebellum tissue lysates (35ug/lane). SCRN3 (arrow) was detected using the purified Pab.
Application
SCRN3 Antibody (C-term) flow cytometric analysis of K562 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.| Application Notes | WB:1:100~500 FC |
|---|
| 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 A column, followed by peptide affinity purification. |
