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Antibody used in IHC on Human kidney.
Antibody used in WB on Human Jurkat 0.2-1 ug/ml.
Antibody used in IHC on Human kidney.

ALDH3A2 Antibody

CATALOG NUMBER: 29-975

Clonality:
Polyclonal
Tested Applications:
ELISA, IHC, WB
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ALDH3A2.
Conjugate:
Unconjugated
Tested Applications:
ELISA, IHC, WB
Application Note:
ALDH3A2 antibody can be used for detection of ALDH3A2 by ELISA at 1:312500. ALDH3A2 antibody can be used for detection of ALDH3A2 by western blot at 0.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Cat. No. 1205 - Jurkat Cell Lysate
Predicted Molecular Weight:
53 kDa, 58 kDa
Purification:
Antibody is purified by peptide affinity chromatography method.
Clonality:
Polyclonal
physical-state:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store ALDH3A2 antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
ALDH3A2
Additional Names:
ALDH3A2, ALDH10, DKFZp686E23276, FALDH, SLS
Protein Accession Number:
NP_000373
Protein Gi Number:
4557303
Ncbi Gene Id Number:
224
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. ALDH3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid.Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome.
Background Reference 1:
Carney, G., Hum. Mutat. 24 (2), 186 (2004).

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

29-975

List Size:
100 ul

List Price:

$519.00

Datasheet
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