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C21orf62 antibody (Biotin)

This Rabbit Polyclonal antibody specifically detects C21orf62 in WB and IHC (p). It exhibits reactivity toward Human, Rat and Mouse.
Catalog No. ABIN1405723

Quick Overview for C21orf62 antibody (Biotin) (ABIN1405723)

Target

C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))

Reactivity

Human, Rat, Mouse

Host

  • 16
  • 2
Rabbit

Clonality

  • 16
  • 2
Polyclonal

Conjugate

  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C21orf62 antibody is conjugated to Biotin

Application

  • 17
  • 13
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C21ORF62

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    IHC-P 1:200-400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C for 12 months.

    Expiry Date

    12 months
  • Target

    C21orf62 (Chromosome 21 Open Reading Frame 62 (C21orf62))

    Alternative Name

    C21ORF62

    Background

    Synonyms: B37, C21orf120, Chromosome 21 open reading frame 62, Hypothetical protein LOC56245, PRED81, Uncharacterized protein C21orf62, CU062_HUMAN.

    Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf62 gene product has been provisionally designated C21orf62 pending further characterization.

    Gene ID

    56245
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