FAM107A anticorps

N° du produit ABIN7236939

Détail du produit anti-FAM107A anticorps

Antigène: FAM107A (Family with Sequence Similarity 107, Member A (FAM107A))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM107A est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of human FAM107A

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.7 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur FAM107A

Antigène: FAM107A (Family with Sequence Similarity 107, Member A (FAM107A))

Autre désignation: FAM107A (FAM107A Produits)

Synonymes: anticorps drr1, anticorps tu3a, anticorps xdrr1, anticorps DRR1, anticorps TU3A, anticorps Drr1, anticorps RGD1306327, anticorps Tu3a, anticorps family with sequence similarity 107 member A S homeolog, anticorps family with sequence similarity 107 member A, anticorps family with sequence similarity 107, member A, anticorps fam107a.S, anticorps FAM107A, anticorps Fam107a

Sujet: FAM107B is a 131 amino acid protein that is encoded by a gene that maps to human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.

UniProt: O95990