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HCCS antibody (Middle Region)

This anti-HCCS antibody is a Rabbit Polyclonal antibody detecting HCCS in WB and IHC (p). Suitable for Human and Mouse.
Catalog No. ABIN952686

Quick Overview for HCCS antibody (Middle Region) (ABIN952686)

Target

See all HCCS Antibodies
HCCS (Holocytochrome C Synthase (HCCS))

Reactivity

  • 43
  • 40
  • 23
  • 6
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 52
  • 6
Rabbit

Clonality

  • 55
  • 3
Polyclonal

Conjugate

  • 32
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  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
This HCCS antibody is un-conjugated

Application

  • 34
  • 20
  • 19
  • 13
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  • 8
  • 7
  • 7
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  • 3
  • 1
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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Binding Specificity

    • 15
    • 9
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    • 4
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    • 1
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    AA 179-209, Middle Region

    Specificity

    This antibody recognizes Human and Mouse HCCS / CCHL (Center).

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 179~209 amino acids from the Central region of human HCCS / CCHL

    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 containing 0.09 % (W/V) Sodium Azide as preservative

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

    HCCS (Holocytochrome C Synthase (HCCS))

    Alternative Name

    HCCS / CCHL

    Background

    The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene.Synonyms: Cytochrome c-type heme lyase, Holocytochrome c-type synthase

    Molecular Weight

    30602 Da

    Gene ID

    3052

    NCBI Accession

    NP_001116080
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