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LOR antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects LOR in WB, ICC, IHC (p) and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7464543

Quick Overview for LOR antibody (N-Term) (ABIN7464543)

Target

See all LOR Antibodies
LOR (Loricrin (LOR))

Reactivity

  • 26
  • 3
  • 1
Human

Host

  • 25
  • 4
Rabbit

Clonality

  • 25
  • 4
Polyclonal

Conjugate

  • 15
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
This LOR antibody is un-conjugated

Application

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  • 6
  • 4
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  • 1
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Western Blotting (WB), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
  • Binding Specificity

    • 15
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    N-Term

    Cross-Reactivity

    Human, Mouse

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of human Loricrin. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: HeLa

    Validation: Orthogonal

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.24 mg/mL

    Buffer

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.025 % ProClin 300

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    LOR (Loricrin (LOR))

    Alternative Name

    loricrin

    Background

    Loricrin,This gene encodes loricrin, a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells. Mutations in this gene are associated with Vohwinkel's syndrome and progressive symmetric erythrokeratoderma, both inherited skin diseases. [provided by RefSeq]

    Molecular Weight

    26 kDa

    Gene ID

    4014

    UniProt

    P23490
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