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ZN673 Antibody (C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, E |
|---|---|
| Primary Accession | Q5JUW0 |
| Other Accession | NP_001123372.1, NP_001123371.1 |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 20100 Da |
| Antigen Region | 96-125 aa |
| Gene ID | 55634 |
|---|---|
| Other Names | KRAB domain-containing protein 4, KRAB box domain-containing protein 4, KRBOX4, ZNF673 |
| Target/Specificity | This ZN673 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 96-125 amino acids from the C-terminal region of human ZN673. |
| Dilution | WB~~1:1000 E~~Use at an assay dependent concentration. |
| 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 | ZN673 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
| Name | KRBOX4 |
|---|---|
| Synonyms | ZNF673 |
| Tissue Location | Expressed in brain, ovary, testis, prostate, tonsil, heart, bone marrow, colon, breast and kidney |
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
ZNF673 belongs to the krueppel C2H2-type zinc-finger protein family. ZNF673 may be involved in transcriptional regulation. Defects in ZNF673 may be the cause of mental retardation X-linked type 92 (MRX92). Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Non-syndromic mental retardation patients do not manifest other clinical signs.
References
Lugtenberg, D., et al. Am. J. Hum. Genet. 78(2):265-278(2006)
Ross, M.T., et al. Nature 434(7031):325-337(2005)
Thiselton, D.L., et al. Genomics 79(4):560-572(2002)
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