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LRPPRC antibody

This anti-LRPPRC antibody is a Rabbit Polyclonal antibody detecting LRPPRC in WB, IHC, ELISA, IF and IP. Suitable for Human, Mouse and Rat.
Catalog No. ABIN5703369

Quick Overview for LRPPRC antibody (ABIN5703369)

Target

See all LRPPRC Antibodies
LRPPRC (Leucine-Rich PPR-Motif Containing (LRPPRC))

Reactivity

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Human, Mouse, Rat

Host

  • 40
Rabbit

Clonality

  • 40
Polyclonal

Conjugate

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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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This LRPPRC antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • Purpose

    LRPPRC antibody

    Immunogen

    leucine-rich PPR-motif containing

    Isotype

    IgG
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    HepG2 cells were subjected to SDS PAGE followed by western blot with FNab04850(LRPPRC antibody) at dilution of 1:500

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Storage Comment

    -20°C for 12 months

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    LRPPRC

    Background

    Synonyms: Leucine-rich PPR motif-containing protein, mitochondrial|130 kDa leucine-rich protein (LRP 130)|GP130|LRPPRC|LRP130

    Background: 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.

    Molecular Weight

    130 kDa

    Gene ID

    10128

    UniProt

    P42704
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