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Mouse Monoclonal ALDH3A2 antibody (STJ98463)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB
Recommended dilution: WB 1:1000-1:2000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
ALDH3A2 antibody, ALDH10 antibody, FALDH antibody,|Ahd 3 antibody|Ahd 3r antibody|Ahd3 antibody|Ahd3 r antibody|AL3A2_HUMAN antibody|Aldehyde dehydrogenase 10 antibody|Aldehyde dehydrogenase 3 antibody|Aldehyde dehydrogenase 3 family, member A2 antibody|Aldehyde dehydrogenase family 3 member A2 antibody|Aldehyde dehydrogenase family 3, subfamily A2 antibody|Aldehyde dehydrogenase, family 3, subfamily A, member 2 antibody|ALDH10 antibody|Aldh3 antibody|ALDH3A2 antibody|Aldh4 antibody|Aldh4 r antibody|Aldh4r antibody|DKFZp686E23276 antibody|FALDH antibody|Fatty aldehyde dehydrogenase antibody|FLJ20851 antibody|Microsomal aldehyde dehydrogenase antibody|msALDH antibody|SLS antibody|Anti-Aldehyde dehydrogenase 10 antibody [EPR15425(B)] (ab184171)
SCBT cat No: sc-373921|
ALDH3A2 Monoclonal Antibody
|Catalogue No.|| |
Human, Mouse, Rat, Rabbit
ALDH3A2 Monoclonal Antibody detects endogenous levels of ALDH3A2 protein.
Purified recombinant human ALDH3A2 protein fragments expressed in Ecoli
|Recommended dilution|| |
ALDH3A2 Antibody was tube-contained. Purified in buffer containing 0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 50% glycerol.
ALDH3A2 Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Fatty aldehyde dehydrogenase antibody, Aldehyde dehydrogenase 10 antibody, Aldehyde dehydrogenase family 3 member A2 antibody, Microsomal aldehyde dehydrogenase antibody
|Protein names|| |
Fatty aldehyde dehydrogenase , Aldehyde dehydrogenase 10 , Aldehyde dehydrogenase family 3 member A2 , Microsomal aldehyde dehydrogenase
|Protein function|| |
Catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Active on a variety of saturated and unsaturated aliphatic aldehydes between 6 and 24 carbons in length. Responsible for conversion of the sphingosine 1-phosphate (S1P) degradation product hexadecenal to hexadecenoic acid. / An aldehyde + NAD+ + H2O = a carboxylate + NADH.
|Involvement in disease|| |
Sjoegren-Larsson syndrome (SLS) [MIM:270200]: An autosomal recessive neurocutaneous disorder characterized by a combination of severe mental retardation, spastic di- or tetraplegia and congenital ichthyosis. Ichthyosis is usually evident at birth with varying degrees of erythema and scaling, neurologic symptoms appear in the first or second year of life. Most patients have an IQ of less than 60. Additional clinical features include glistening white spots on the retina, seizures, short stature and speech defects. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the aldehyde dehydrogenase family.
|Protein cellular localization|| |
Endoplasmic reticulum membrane; Single-pass membrane protein; Cytoplasmic side
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St John’s Laboratory Ltd.
|Product type|| |
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