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HRAS antibody (AA 104-128)

The Rabbit Polyclonal anti-HRAS antibody has been validated for WB, ELISA, IHC and IF. It is suitable to detect HRAS in samples from Human.
Catalog No. ABIN3029525

Quick Overview for HRAS antibody (AA 104-128) (ABIN3029525)

Target

See all HRAS Antibodies
HRAS (HRas proto-oncogene, GTPase (HRAS))

Reactivity

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  • 53
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This HRAS antibody is un-conjugated

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

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    AA 104-128

    Cross-Reactivity (Details)

    Expected species reactivity: Mouse, Rat

    Purification

    Purified

    Immunogen

    A portion of amino acids 104-128 from the human protein was used as the immunogen for this HRAS antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the HRAS antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:500-1000,IHC (Paraffin): 1:10-1:50,Immunofluorescence: 1:10-1:50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Aliquot the HRAS antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    HRAS (HRas proto-oncogene, GTPase (HRAS))

    Alternative Name

    HRAS

    Background

    HRAS belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. These proteins function in signal transduction pathways. They can bind GTP and GDP, and they have intrinsic GTPase activity. HRAS undergoes a continuous cycle of de- and re-palmitoylation, which regulates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, mental retardation, skin and musculoskeletal abnormalities, distinctive facial appearance and cardiovascular abnormalities. Defects in the HRAS gene are implicated in a variety of cancers, including bladder cancer, follicular thyroid cancer, and oral squamous cell carcinoma.

    UniProt

    P01112

    Pathways

    p53 Signaling, MAPK Signaling, RTK Signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Hepatitis C, Autophagy, Signaling Events mediated by VEGFR1 and VEGFR2, Signaling of Hepatocyte Growth Factor Receptor, Regulation of long-term Neuronal Synaptic Plasticity, VEGF Signaling, BCR Signaling
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