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Indian Hedgehog antibody (N-Term)

This anti-Indian Hedgehog antibody is a Rabbit Polyclonal antibody detecting Indian Hedgehog in WB and EIA. Suitable for Human.
Catalog No. ABIN952896

Quick Overview for Indian Hedgehog antibody (N-Term) (ABIN952896)

Target

See all Indian Hedgehog (IHH) Antibodies
Indian Hedgehog (IHH)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Indian Hedgehog antibody is un-conjugated

Application

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Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

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    AA 50-80, N-Term

    Specificity

    This antibody detects Indian hedgehog protein / IHH.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human

    Purification

    Purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    Synthetic peptide - KLH conjugated - corresponding to the N-terminal region (between 50-80aa) of human Indian hedgehog protein / IHH.

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS with 0.09 % (W/V) 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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    Indian Hedgehog (IHH)

    Alternative Name

    Indian Hedgehog Protein / IHH

    Background

    The IHH gene encodes a member of the hedgehog family of secreted signaling molecules. Hedgehog proteins are essential regulators of a variety of developmental processes including growth, patterning and morphogenesis. The encoded protein specifically plays a role in bone growth an differentiation. Mutations in this gene are the cause of brachydactyly type A1 which is characterized by shortening or malformation of the phalanges. Mutations in this gene are also the cause of acrocapitofemoral dysplasia.Synonyms: HHG-2, HHG2

    Gene ID

    3549

    NCBI Accession

    NP_002172

    Pathways

    Hedgehog Signaling
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