Anti-Human ALDH7A1 Antibody [A1179] with collaborator-tested evidence for Flow Cyt, ICC/IF.
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Anti-Human ALDH7A1 Antibody [A1179] is a research-use antibody from Elabscience for studying ALDH7A1 in Flow Cytometry, IF/ICC workflows with listed reactivity for Human. Specifications and supporting documents below should be reviewed when planning the experiment.
Fully tested in-house by ABMIUM. Highest confidence. Non-conformities fully supported under the ABMIUM Product Promise.
Quality verified. Independent collaborator or expected-performance data available. Product meets ABMIUM quality standards.
Expected to work based on structural and biochemical data. Not yet directly tested by ABMIUM or a collaborator. No non-conformity support for this combination.
Not recommended for this application or species/sample combination. This may indicate either evidence of unsuitability or that the combination has not been tested and therefore cannot currently be recommended.
Evidence status by application and model.
| Species | WB | IHC-P | IHC-Fr | IF/ICC | Flow Cyt | IP | ChIP | ICC/IF |
|---|---|---|---|---|---|---|---|---|
| Human |
This product is manufactured by Elabscience and sold through ABMIUM without relabelling.
ABMIUM supports global orders. Availability, shipping requirements and applicable import arrangements are confirmed before fulfilment where required.
Yes. Send your target, sample, application and experimental conditions through ABMIUM MATCH or technical support.
Unless the listing expressly states otherwise, ABMIUM products are supplied for research use only and are not for diagnostic or therapeutic use.
ALDH7A1 (aldehyde dehydrogenase 7 family member A1), also known as alpha-aminoadipic semialdehyde dehydrogenase or antiquitin, is a cytosolic and mitochondrial aldehyde dehydrogenase. Researchers study ALDH7A1 in aldehyde detoxification, lysine-degradation biology and pyridoxine-dependent epilepsy.
Biological function: ALDH7A1 is an aldehyde dehydrogenase with cytosolic and mitochondrial isoforms. It protects cells from oxidative stress by metabolising lipid-peroxidation-derived aldehydes and is also linked to the alpha-aminoadipic semialdehyde step of human lysine degradation.
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