DHX9 antibody (AA 396-759)

Catalog No. ABIN7874648

This Rabbit Polyclonal antibody specifically detects DHX9 in WB, ELISA, IF, IP, FACS and IHC (p). It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for DHX9 antibody (AA 396-759) (ABIN7874648)

Target: DHX9 (ATP-Dependent RNA Helicase A (DHX9))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DHX9 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-DHX9 Antibody

Binding Specificity: AA 396-759

Purpose: RNA Helicase A Antibody / DHX9

Purification: Affinity purified

Immunogen: Recombinant human protein (amino acids E396-E759) was used as the immunogen for the RNA Helicase A antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the RNA Helicase A antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the RNA Helicase A antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for DHX9

Target: DHX9 (ATP-Dependent RNA Helicase A (DHX9))

Alternative Name: RNA Helicase A

Background: ATP-dependent RNA helicase A (RHA, also known as DHX9, LKP, and NDHI) is an enzyme that in humans is encoded by the DHX9 gene. It is mapped to 1q25.3. This gene encodes a member of the DEAH-containing family of RNA helicases. The encoded protein is an enzyme that catalyzes the ATP-dependent unwinding of double-stranded RNA and DNA-RNA complexes. This protein localizes to both the nucleus and the cytoplasm and functions as a transcriptional regulator. This protein may also be involved in the expression and nuclear export of retroviral RNAs. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 11 and 13.

UniProt: Q08211