PIMA531616

ALDH6A1 Monoclonal Antibody (6H9B8), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA531616-Each-of-1 In Stock ₹ 49,350.50

PIMA531616 - Each of 1

₹ 49,350.50

In Stock

Quantity

1

Base Price: ₹ 49,350.50

GST (18%): ₹ 8,883.09

Total Price: ₹ 58,233.59

Antigen

ALDH6A1

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

PBS with 0.05% sodium azide

Gene Accession No.

Q02252

Gene Symbols

ALDH6A1

Immunogen

Purified recombinant fragment of human ALDH6A1 (AA: 1-195) expressed in E. coli.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG1

Applications

ELISA, Flow Cytometry, Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Clone

6H9B8

Conjugate

Unconjugated

Gene

ALDH6A1

Gene Alias

1110038I05Rik; AI314632; aldehyde dehydrogenase 6 family member A1; aldehyde dehydrogenase 6 family, member A1; aldehyde dehydrogenase family 6 member A1; aldehyde dehydrogenase family 6, subfamily A1; Aldh6a1; malonate-semialdehyde dehydrogenase; methylmalonate semialdehyde dehydrogenase; methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial; MGC40271; mitochondrial acylating methylmalonate-semialdehyde dehydrogenase; MMSADHA; Mmsdh; testicular tissue protein Li 122

Host Species

Mouse

Purification Method

Protein G

Regulatory Status

RUO

Gene ID (Entrez)

4329

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

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Description

  • MA5-31616 has been tested in indirect ELISA
  • 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.