PIPA530090

ALDH6A1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA530090-Each-of-1 In Stock ₹ 46,502.50

PIPA530090 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

ALDH6A1

Classification

Polyclonal

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

Rabbit

Purification Method

Antigen affinity chromatography

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

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

0.63 mg/mL

Formulation

PBS with 1% BSA, 20% glycerol and 0.01% thimerosal; pH 7

Gene Accession No.

Q02252

Gene Symbols

ALDH6A1

Immunogen

Recombinant fragment corresponding to a region within amino acids 1 and 255 of Human ALDH6A1

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • Recommended positive controls: 293T, A431, Jurkat
  • Predicted reactivity: Mouse (93%), Rat (92%), Bovine (90%)
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • 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.