HAGH Antibody (C-term) (Ascites)
Mouse Monoclonal Antibody (Mab)
- 产品详情
- 实验流程
- 背景知识
Application ![]()
| WB, E |
---|---|
Primary Accession | Q16775 |
Other Accession | NP_005317.2 |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Isotype | IgG1 |
Clone Names | 611CT23.6.1 |
Calculated MW | 33806 Da |
Antigen Region | 279-308 aa |
Gene ID | 3029 |
---|---|
Other Names | Hydroxyacylglutathione hydrolase, mitochondrial, Glyoxalase II, Glx II, HAGH, GLO2, HAGH1 |
Target/Specificity | This HAGH antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 279-308 amino acids from the C-terminal region of human HAGH. |
Dilution | WB~~1:100~1600 E~~Use at an assay dependent concentration. |
Format | Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide. |
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 | HAGH Antibody (C-term) (Ascites) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | HAGH |
---|---|
Synonyms | GLO2, HAGH1 |
Function | Thiolesterase that catalyzes the hydrolysis of S-D-lactoyl- glutathione to form glutathione and D-lactic acid. |
Cellular Location | [Isoform 1]: Mitochondrion matrix |
Tissue Location | Expressed in liver and kidney. |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
The enzyme encoded by this gene is classified as a thiolesterase and is responsible for the hydrolysis of S-lactoyl-glutathione to reduced glutathione and D-lactate. Two transcript variants encoding different isoforms have been found for this gene.
REFERENCES
Davila, S., et al. Genes Immun. 11(3):232-238(2010)
Limphong, P., et al. Biochemistry 48(23):5426-5434(2009)
Antognelli, C., et al. Cancer Biol. Ther. 6(12):1880-1888(2007)
Xu, Y., et al. J. Biol. Chem. 281(36):26702-26713(2006)
Antognelli, C., et al. Cancer J 12(3):222-228(2006)

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