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CYB5A antibody (AA 69-98)

This anti-CYB5A antibody is a Rabbit Polyclonal antibody detecting CYB5A in WB and IHC (p). Suitable for Human.
Catalog No. ABIN657954

Quick Overview for CYB5A antibody (AA 69-98) (ABIN657954)

Target

See all CYB5A Antibodies
CYB5A (Cytochrome B5 Type A (Microsomal) (CYB5A))

Reactivity

  • 35
  • 12
  • 11
Human

Host

  • 30
  • 6
Rabbit

Clonality

  • 31
  • 4
Polyclonal

Conjugate

  • 17
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CYB5A antibody is un-conjugated

Application

  • 25
  • 22
  • 15
  • 8
  • 7
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB34066
  • Binding Specificity

    • 6
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 69-98

    Purification

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

    Immunogen

    This CYB5A antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 69-98 amino acids from the Central region of human CYB5A.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. WB: 1:1000. IHC-P: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody 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

    CYB5A Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Expiry Date

    6 months
  • Target

    CYB5A (Cytochrome B5 Type A (Microsomal) (CYB5A))

    Alternative Name

    CYB5A

    Background

    The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    15330

    Gene ID

    1528

    NCBI Accession

    NP_001177736, NP_001905, NP_683725

    UniProt

    P00167
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