PTRHD1 anticorps (AA 1-140)

N° du produit ABIN7598993

Cet anticorps anti-PTRHD1 est un anticorps Lapin Polyclonal détectant PTRHD1 dans WB, ELISA, ICC, FACS, IF et IHC. Adapté pour Souris, Rat et Humain.

Aperçu rapide pour PTRHD1 anticorps (AA 1-140) (ABIN7598993)

Antigène: PTRHD1 (Peptidyl-tRNA Hydrolase Domain Containing 1 (PTRHD1))

Reactivité: Souris, Rat, Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PTRHD1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS), Immunofluorescence (IF), Immunohistochemistry (IHC)

Détail du produit anti-PTRHD1 anticorps

Épitope: AA 1-140

Fonction: Anti-PTRHD1 Antibody Picoband®

Attributs du produit: Anti-PTRHD1 Antibody Picoband® (ABIN7598993). Tested in WB, IHC, ICC/IF, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human C2orf79/PTRHD1 recombinant protein (Position: M1-K140). Human C2orf79/PTRHD1 shares 89.3% amino acid (aa) sequence identity with mouse C2orf79/PTRHD1.

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human
Immunohistochemistry, 2-5 μg/mL, Mouse, Rat
Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/mL, -
1. Al-Kasbi, G., Al-Saegh, A., Al-Qassabi, A., Al-Jabry, T., Zadjali, F., Al-Yahyaee, S., Al-Maawali, A. Biallelic PTRHD1 frameshift variants associated with intellectual disability, spasticity, and parkinsonism. Mov. Disord. Clin. Pract. 8: 1253-1257, 2021. 2. Cheraghi, S., Moghbelinejad, S., Najmabadi, H., Kahrizi, K., Najafipour, R. The PTRHD1 mutation in intellectual disability. Arch. Iran. Med. 24: 747-751, 2021. 3. Elahi, E. PTRHD1 and possibly ADORA1 mutations contribute to Parkinsonism with intellectual disability. Mov. Disord. 33: 174, 2018.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Détails sur PTRHD1

Antigène: PTRHD1 (Peptidyl-tRNA Hydrolase Domain Containing 1 (PTRHD1))

Autre désignation: PTRHD1

Sujet: This gene encodes the enzyme peptidyl-tRNA hydrolase. Peptidyl-tRNA hydrolases perform the essential function of recycling peptidyl-tRNAs. Mutations in this gene are associated with autosomal-recessive intellectual disability and parkinsonism.

Poids moléculaire: 16 kDa

ID gène: 391356