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DRAK1 Antibody (N-term)
Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | Q9UEE5 |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 46558 Da |
| Antigen Region | 1-30 aa |
| Gene ID | 9263 |
|---|---|
| Other Names | Serine/threonine-protein kinase 17A, DAP kinase-related apoptosis-inducing protein kinase 1, STK17A, DRAK1 |
| Target/Specificity | This DRAK1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human DRAK1. |
| Dilution | WB~~1:1000 |
| Format | 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. |
| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
| Precautions | DRAK1 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | STK17A |
|---|---|
| Synonyms | DRAK1 |
| Function | Acts as a positive regulator of apoptosis. Also acts as a regulator of cellular reactive oxygen species. |
| Cellular Location | Nucleus. |
| Tissue Location | Highly expressed in placenta. Lower levels in heart, lung, skeletal muscle, kidney and pancreas |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Background
DRAK1 is a member of the DAP kinase-related apoptosis-inducing protein kinase family and encodes an autophosphorylated nuclear protein with a protein kinase domain. The protein has apoptosis-inducing activity.
References
Sanjo, H., et al., J. Biol. Chem. 273(44):29066-29071 (1998).
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