Application
Formalin-fixed and paraffin-embedded human hepatocarcinoma tissue reacted with JMJD4 (C-term) , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.Application
Western blot analysis of anti-JMJD4 (C-term) Pab in Hela and mouse kidney cell line lysate. JMJD4 (C-term)(arrow) was detected using the purified Pab.| Product Name | JMJD4 Antibody (C-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | JMJD4; JmjC domain-containing protein 4; Jumonji domain-containing protein 4 |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | IHCWB |
| IHC:1:10~50 WB |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Alternative Names | JMJD4 JmjC domain-containing protein 4 Jumonji domain-containing protein 4 |
|---|---|
| Molecular Weight(MW) | 52493 Da |
| Tissue Specificity | This JMJD4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 432~461 amino acids from the C-terminal region of human JMJD4. |
| Entrez Gene | 65094 |
|---|
Application
Formalin-fixed and paraffin-embedded human hepatocarcinoma tissue reacted with JMJD4 (C-term) , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
Application
Western blot analysis of anti-JMJD4 (C-term) Pab in Hela and mouse kidney cell line lysate. JMJD4 (C-term)(arrow) was detected using the purified Pab.| Application Notes | IHC:1:10~50 WB |
|---|
| 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. |
