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CRTAP antibody (N-Term)

This anti-CRTAP antibody is a Rabbit Polyclonal antibody detecting CRTAP in WB and IF. Suitable for Human.
Catalog No. ABIN5532526

Quick Overview for CRTAP antibody (N-Term) (ABIN5532526)

Target

See all CRTAP Antibodies
CRTAP (Cartilage Associated Protein (CRTAP))

Reactivity

  • 38
  • 10
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
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  • 1
  • 1
Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This CRTAP antibody is un-conjugated

Application

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  • 9
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  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

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    AA 31-59, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This CRTAP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 31-59 amino acids from the N-terminal region of human CRTAP.

    Isotype

    Ig Fraction
  • Application Notes

    For IF starting dilution is: 1:25

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Supplied in 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.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    CRTAP (Cartilage Associated Protein (CRTAP))

    Alternative Name

    CRTAP

    Background

    The protein encoded by this gene is similar to the chicken and mouse CRTAP genes. The encoded protein is a scaffolding protein that may influence the activity of at least one member of the cytohesin/ARNO family in response to specific cellular stimuli. Defects in this gene are associated with osteogenesis imperfecta, a connective tissue disorder characterized by bone fragility and low bone mass.

    Molecular Weight

    47 kDa

    Gene ID

    10491

    UniProt

    O75718
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