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ALDH6A1 antibody
ALDH6A1
Reactivity: Human
WB, IHC (p), IF
Host: Mouse
Monoclonal
147CT8-3-4
unconjugated
Product Details anti-ALDH6A1 Antibody
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Target
See all ALDH6A1 Antibodies
ALDH6A1
(Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))
Reactivity
All reactivities for ALDH6A1 antibodies
Human
Host
All hosts for ALDH6A1 antibodies
Mouse
Clonality
All clonalities for ALDH6A1 antibodies
Monoclonal
Conjugate
All conjugates for ALDH6A1 antibodies
This ALDH6A1 antibody is un-conjugated
Application
All applications for ALDH6A1 antibodies
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
Purification
This antibody is purified through a protein G column, followed by dialysis against PBS.
Immunogen
This ALDH6A1 antibody is generated from mouse immunized with ALDH6A1 recombinant protein.
Clone
147CT8-3-4
Isotype
IgG1, Ig kappa
Top Product
Discover our top product ALDH6A1 Primary Antibody
Alternatives
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Application Details
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Application Notes
IF: 1:25. WB: 1:1000. IHC-P: 1:25. IHC-P: 1:25
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Purified monoclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C,-20 °C
Storage Comment
Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
Expiry Date
6 months
Target Details for ALDH6A1
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Target
ALDH6A1
(Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))
Alternative Name
ALDH6A1 (ALDH6A1 Products )
Background
This protein belongs to the aldehyde dehydrogenases family of proteins. This enzyme plays a role in the valine and pyrimidine catabolic pathways. The product of this gene, a mitochondrial methylmalonate semialdehyde dehydrogenase, catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids.
Molecular Weight
57840
Gene ID
4329
NCBI Accession
NP_005580
UniProt
Q02252
Pathways
Brown Fat Cell Differentiation
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