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Mouse Anti-ALDH6A1 Recombinant Antibody (6H9B7) (CBMAB-A2300-YC)

Provided herein is a Mouse monoclonal antibody against Human Aldehyde Dehydrogenase 6 Family Member A1. The antibody can be used for immunoassay techniques, such as WB, FC, ELISA, IHC.
See all ALDH6A1 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
6H9B7
Antibody Isotype
IgG1
Application
WB, FC, ELISA, IHC, IF

Basic Information

Immunogen
Purified recombinant fragment of human ALDH6A1 (aa 1-195) expressed in E. Coli
Host Species
Mouse
Specificity
Human
Antibody Isotype
IgG1
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.
ApplicationNote
IF(ICC)1:200-1:1,000
ELISA1:10,000
WB1:500-1:2,000
IHC-P1:200-1:1,000
FC1:200-1:400

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS
Preservative
0.05% sodium azide
Concentration
1 mg/ml
Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Aldehyde Dehydrogenase 6 Family Member A1
Introduction
ALDH6A1 is a member of the aldehyde dehydrogenase protein family. The encoded protein is a mitochondrial methylmalonate semialdehyde dehydrogenase that plays a role in the valine and pyrimidine catabolic pathways. This protein catalyzes the irreversible o
Entrez Gene ID
UniProt ID
Alternative Names
Aldehyde Dehydrogenase 6 Family Member A1; MMSDH; Methylmalonate-Semialdehyde Dehydrogenase [Acylating], Mitochondrial; Mitochondrial Acylating Methylmalonate-Semialdehyde Dehydrogenase; Malonate-Semialdehyde Dehydrogenase [Acylating]; Aldehyde Dehydrogen
Function
Plays a role in valine and pyrimidine metabolism. Binds fatty acyl-CoA.
Biological Process
Branched-chain amino acid catabolic process Source: Reactome
Brown fat cell differentiation Source: Ensembl
Thymine catabolic process Source: BHF-UCL
Thymine metabolic process Source: UniProtKB
Valine catabolic process Source: BHF-UCL
Valine metabolic process Source: UniProtKB
Cellular Location
Mitochondrion
Involvement in disease
Methylmalonate semialdehyde dehydrogenase deficiency (MMSDHD): A metabolic disorder characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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