PTRHD1 Antikörper (AA 1-140)

Produktnummer ABIN7598993

Dieses Anti-PTRHD1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von PTRHD1 in WB, ELISA, ICC, FACS, IF und IHC. Geeignet für Maus, Ratte und Human.

Kurzübersicht für PTRHD1 Antikörper (AA 1-140) (ABIN7598993)

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

Reaktivität: Maus, Ratte, Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PTRHD1 Antikörper ist unkonjugiert

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

Produktdetails anti-PTRHD1 Antikörper

Bindungsspezifität: AA 1-140

Verwendungszweck: Anti-PTRHD1 Antibody Picoband®

Produktmerkmale: 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.

Aufreinigung: Immunogen affinity purified.

Immunogen: 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.

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

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

Konzentration: 500 μg/mL

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu PTRHD1

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

Andere Bezeichnung: PTRHD1

Hintergrund: 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.

Molekulargewicht: 16 kDa

Gen-ID: 391356