ALDOA Antibody (monoclonal) (M02)
Mouse monoclonal antibody raised against a full length recombinant ALDOA.
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- 文献引用 : 1
- 实验流程
- 背景知识
Application ![]()
| WB, IF |
---|---|
Primary Accession | P04075 |
Other Accession | BC010660 |
Reactivity | Human |
Host | mouse |
Clonality | monoclonal |
Isotype | IgG1 kappa |
Clone Names | 3C12-6D11 |
Calculated MW | 39420 Da |
Gene ID | 226 |
---|---|
Other Names | Fructose-bisphosphate aldolase A, Lung cancer antigen NY-LU-1, Muscle-type aldolase, ALDOA, ALDA |
Target/Specificity | ALDOA (AAH10660.1, 1 a.a. ~ 364 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. |
Dilution | WB~~1:500~1000 IF~~1:50~200 |
Format | Clear, colorless solution in phosphate buffered saline, pH 7.2 . |
Storage | Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. |
Precautions | ALDOA Antibody (monoclonal) (M02) is for research use only and not for use in diagnostic or therapeutic procedures. |
For Research Use Only. Not For Use In Diagnostic Procedures.

Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
This gene product, Aldolase A (fructose-bisphosphate aldolase) is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing of this gene results in multiple transcript variants which encode the same protein.
REFERENCES
1.Grade-dependent proteomic characterization of kidney cancer.Perroud B, Ishimaru T, Borowsky AD, Weiss RH.Mol Cell Proteomics. 2009 May;8(5):971-85. Epub 2009 Jan 21.

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