PTRHD1 antibody (AA 1-140)

Catalog No. ABIN7598993

This anti-PTRHD1 antibody is a Rabbit Polyclonal antibody detecting PTRHD1 in WB, ELISA, ICC, FACS, IF and IHC. Suitable for Mouse, Rat and Human.

Quick Overview for PTRHD1 antibody (AA 1-140) (ABIN7598993)

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

Reactivity: Mouse, Rat, Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PTRHD1 antibody is un-conjugated

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

Product Details anti-PTRHD1 Antibody

Binding Specificity: AA 1-140

Purpose: Anti-PTRHD1 Antibody Picoband®

Characteristics: 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.

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.

Application Details

Application Notes: 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

Handling

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.

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for PTRHD1

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

Alternative Name: PTRHD1

Background: 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.

Molecular Weight: 16 kDa

Gene ID: 391356