AASS anticorps (Middle Region)

N° du produit ABIN357942

Détail du produit anti-AASS anticorps

Antigène: AASS (Aminoadipate Semialdehyde Synthase (AASS))

Épitope: Middle Region

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AASS est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Specificité: This antibody detects AASS (Center).

Purification: Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

Immunogène: This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the center region of human AASS.

Isotype: Ig Fraction

Information d'application

Indications d'application: ELISA: 1/1,000. Immunohistochemistry: 1/50-1/100.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) Sodium Azide as preservative.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.

Détails sur AASS

Antigène: AASS (Aminoadipate Semialdehyde Synthase (AASS))

Autre désignation: AASS (AASS Produits)

Synonymes: anticorps LKR/SDH, anticorps LKRSDH, anticorps LORSDH, anticorps LKR, anticorps LOR, anticorps LOR/SDH, anticorps Lorsdh, anticorps SDH, anticorps aminoadipate-semialdehyde synthase, anticorps AASS, anticorps Aass

Sujet: AASS is a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. The N-terminal and the C-terminal portions of this enzyme contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha-aminoadipic semialdehyde. Mutations in the gene encoding this protein are associated with familial hyperlysinemia.Synonyms: Alpha-aminoadipic semialdehyde synthase, LKR/SDH, mitochondrial

Poids moléculaire: 102001 Da

ID gène: 10157, 9606

UniProt: Q9UDR5

Pathways: SARS-CoV-2 Protein Interactome