LRPPRC antibody (AA 1281-1394)

Catalog No. ABIN7870417

The Rabbit Polyclonal anti-LRPPRC antibody (ABIN7870417) specifically detects LRPPRC in WB, ELISA, IF, IHC (p) and FACS. The antibody is reactive with Human, Mouse, Rat and Monkey samples.

Quick Overview for LRPPRC antibody (AA 1281-1394) (ABIN7870417)

Target: LRPPRC (Leucine-Rich PPR-Motif Containing (LRPPRC))

Reactivity: Human, Mouse, Rat, Monkey

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LRPPRC antibody is un-conjugated

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

Product Details anti-LRPPRC Antibody

Binding Specificity: AA 1281-1394

Purpose: LRPPRC Antibody / GP130

Purification: Affinity purified

Immunogen: Recombinant human protein (amino acids A1281-S1394) was used as the immunogen for the LRPPRC antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the LRPPRC 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 LRPPRC 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 LRPPRC

Target: LRPPRC (Leucine-Rich PPR-Motif Containing (LRPPRC))

Alternative Name: LRPPRC

Background: Leucine-rich PPR motif-containing protein, mitochondrial is a protein that in humans is encoded by the LRPPRC gene. It is mapped to 2p21. This gene encodes a leucine-rich protein that has multiple pentatricopeptide repeats (PPR). The precise role of this protein is unknown but studies suggest it may play a role in cytoskeletal organization, vesicular transport, or in transcriptional regulation of both nuclear and mitochondrial genes. The protein localizes primarily to mitochondria and is predicted to have an N-terminal mitochondrial targeting sequence. Mutations in this gene are associated with the French-Canadian type of Leigh syndrome.

UniProt: P42704