Application
NSUN6 Antibody (C-term) western blot analysis in HL-60,CEM and K562 cell line lysates (35ug/lane).This demonstrates the NSUN6 antibody detected the NSUN6 protein (arrow).Application
NSUN6 Antibody (C-term) flow cytometric analysis of HL-60 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 | NSUN6 Antibody (C-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WBFC |
| WB:1:100~500 FC |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | NOPD1 |
|---|---|
| Alternative Names | NSUN6 NOPD1 Putative methyltransferase NSUN6 NOL1/NOP2/Sun and PUA domain-containing protein 1 NOL1/NOP2/Sun domain family member 6 |
| Molecular Weight(MW) | 51770 Da |
| Function | May have S-adenosyl-L-methionine-dependent methyl- transferase activity (Potential) |
| Tissue Specificity | This NSUN6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 432-461 amino acids from the C-terminal region of human NSUN6. |
| Entrez Gene | 221078 |
|---|---|
| Nucleotide Accession | NP_872349.1 |
Application
NSUN6 Antibody (C-term) western blot analysis in HL-60,CEM and K562 cell line lysates (35ug/lane).This demonstrates the NSUN6 antibody detected the NSUN6 protein (arrow).
Application
NSUN6 Antibody (C-term) flow cytometric analysis of HL-60 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. |
