MOCS1 anticorps (N-Term)

N° du produit ABIN1539287

L’anticorps Lapin Polyclonal anti-MOCS1 a été validé pour WB. Il convient pour détecter MOCS1 dans des échantillons de Humain.

Aperçu rapide pour MOCS1 anticorps (N-Term) (ABIN1539287)

Antigène: MOCS1 (Molybdenum Cofactor Synthesis 1 (MOCS1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MOCS1 est non-conjugé

Application: Western Blotting (WB)

Clone: RB38897

Détail du produit anti-MOCS1 anticorps

Épitope: AA 31-58, N-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This MOCS1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 31-58 amino acids from the N-terminal region of human MOCS1.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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.

Stock: 4 °C,-20 °C

Stockage commentaire: MOCS1 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur MOCS1

Antigène: MOCS1 (Molybdenum Cofactor Synthesis 1 (MOCS1))

Autre désignation: MOCS1

Sujet: Molybdenum cofactor biosynthesis is a conserved pathway leading to the biological activation of molybdenum. The protein encoded by this gene is involved in this pathway. This gene was originally thought to produce a bicistronic mRNA with the potential to produce two proteins (MOCS1A and MOCS1B) from adjacent open reading frames. However, only the first open reading frame (MOCS1A) has been found to encode a protein from the putative bicistronic mRNA, whereas additional splice variants, whose full-length natures have yet to be determined, are likely to produce a fusion between the two open reading frames. This gene is defective in patients with molybdenum cofactor deficiency, type A. A related pseudogene has been identified on chromosome 16.

Poids moléculaire: 70105

ID gène: 4337

NCBI Accession: NP_001068566, NP_005934

UniProt: Q9NZB8