ADCY4 Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application ![]()
| FC, WB, E |
---|---|
Primary Accession | Q8NFM4 |
Other Accession | P26770, Q91WF3 |
Reactivity | Human |
Predicted | Mouse, Rat |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 119794 Da |
Antigen Region | 415-441 aa |
Gene ID | 196883 |
---|---|
Other Names | Adenylate cyclase type 4, ATP pyrophosphate-lyase 4, Adenylate cyclase type IV, Adenylyl cyclase 4, ADCY4 |
Target/Specificity | This ADCY4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 415-441 amino acids from the Central region of human ADCY4. |
Dilution | WB~~1:1000 FC~~1:10~50 |
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 | ADCY4 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | ADCY4 |
---|---|
Function | Catalyzes the formation of the signaling molecule cAMP in response to G-protein signaling. |
Cellular Location | Cell membrane; Multi-pass membrane protein. Cytoplasm |
Tissue Location | Detected in the zona glomerulosa and the zona fasciculata in the adrenal gland (at protein level) |

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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of the family of adenylate cyclases, which are membrane-associated enzymes that catalyze the formation of the secondary messenger cyclic adenosine monophosphate (cAMP). Mouse studies show that adenylate cyclase 4, along with adenylate cyclases 2 and 3, is expressed in olfactory cilia, suggesting that several different adenylate cyclases may couple to olfactory receptors and that there may be multiple receptor-mediated mechanisms for the generation of cAMP signals.
References
Rhim, J.H., et al. Aging Cell 5(6):451-461(2006)
Jiang, G., et al. Am. J. Physiol. Endocrinol. Metab. 284 (4), E671-E678 (2003)
Sunahara, R.K., et al. Mol. Interv. 2(3):168-184(2002)
Ludwig, M.G., et al. J. Recept. Signal Transduct. Res. 22 (1-4), 79-110 (2002)
Cote, M., et al. J. Clin. Endocrinol. Metab. 86(9):4495-4503(2001)

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