Leucine Rich PPR Motif Containing Protein (LRPPRC) Antibody

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Description
LRPPRC Antibody is a Rabbit Polyclonal antibody against LRPPRC. 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.
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Product specifications
Category | Primary Antibodies |
Immunogen Target | Leucine Rich PPR Motif Containing Protein (LRPPRC) |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Recommended Dilution | IHC-P: 1/100 - 1/200, IF/ICC: 1/100 - 1/200. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Purification | Purified by affinity chromatography. |
Size 1 | 60 µl |
Size 2 | 120 µl |
Size 3 | 200 µl |
Form | Liquid |
Tested Applications | IHC, IF/ICC |
Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P42704 |
Gene ID | 10128 |
NCBI Accession | NP_573566.2 |
Background | Antibody anti-LRPPRC |
Status | RUO |
Note | Concentration: 1 mg/ml - |
Descripción
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LRPPRC antibody
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.
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