PIPA558072

ACAD9 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA558072-Each-of-1 In Stock ₹ 52,599.00

PIPA558072 - Each of 1

₹ 52,599.00

In Stock

Quantity

1

Base Price: ₹ 52,599.00

GST (18%): ₹ 9,467.82

Total Price: ₹ 62,066.82

Antigen

ACAD9

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Acad9

Gene Alias

2600017P15Rik; 4732402K02; ACAD9; ACAD-9; Acyl-CoA dehydrogenase family member 9; acyl-CoA dehydrogenase family member 9, mitochondrial; acyl-CoA dehydrogenase family, member 9; acyl-Coenzyme A dehydrogenase family, member 9; C630012L17Rik; Complex I assembly factor ACAD9, mitochondrial; NPD002; Nyggf2; very-long-chain acyl-CoA dehydrogenase VLCAD; very-long-chain acyl-CoA dehydrogenase VLCAD homolog

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

28976

Content And Storage

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

Form

Liquid

Applications

Immunocytochemistry, Immunohistochemistry, Western Blot

Concentration

0.1 mg/mL

Formulation

PBS with 40% glycerol and 0.02% sodium azide; pH 7.2

Gene Accession No.

Q9H845

Gene Symbols

Acad9

Immunogen

Recombinant protein corresponding to Human ACAD9

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • Immunogen sequence: EILRMYIALT GLQHAGRILT TRIHELKQAK VSTVMDTVGR RLRDSLGRTV DLGLTGNHGV VHPSLADSAN KFEENTYCFG RTVETLL Highest antigen sequence identity to the following orthologs: Mouse - 79%, Rat - 77%
  • This gene encodes a member of the acyl-CoA dehydrogenase family
  • Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA
  • The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates
  • Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency
  • Alternate splicing results in multiple transcript variants.