OTC Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
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- 文献引用 : 1
- 实验流程
- 背景知识
Application ![]()
| IHC-P, FC, WB, E |
---|---|
Primary Accession | P00480 |
Other Accession | P00481, O19072, P11725, Q9N1U7 |
Reactivity | Human, Rat, Mouse |
Predicted | Mouse, Rat, Pig, Bovine |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 39935 Da |
Antigen Region | 71-98 aa |
Gene ID | 5009 |
---|---|
Other Names | Ornithine carbamoyltransferase, mitochondrial, Ornithine transcarbamylase, OTCase, OTC |
Target/Specificity | This OTC antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 71-98 amino acids of human OTC. |
Dilution | IHC-P~~N/A FC~~1:10~50 WB~~1:2000 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 | OTC Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | OTC (HGNC:8512) |
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Function | Catalyzes the second step of the urea cycle, the condensation of carbamoyl phosphate with L-ornithine to form L-citrulline (PubMed:2556444, PubMed:6372096, PubMed:8112735). The urea cycle ensures the detoxification of ammonia by converting it to urea for excretion (PubMed:2556444). |
Cellular Location | Mitochondrion matrix |
Tissue Location | Mainly expressed in liver and intestinal mucosa. |
Research Areas
For Research Use Only. Not For Use In Diagnostic Procedures.

Application Protocols
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
OTC is a mitochondrial matrix enzyme. Missense, nonsense, and frameshift mutations in this enzyme lead to ornithine transcarbamylase deficiency, which causes hyperammonemia.
REFERENCES
Hansmannel,F., et.al., Neurosci. Lett. 449 (1), 76-80 (2009)

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