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CMSS1 antibody (Cy5.5)

The Rabbit Polyclonal anti-CMSS1 antibody has been validated for WB. It is suitable to detect CMSS1 in samples from Human, Mouse and Rat.
Catalog No. ABIN1705658

Quick Overview for CMSS1 antibody (Cy5.5) (ABIN1705658)

Target

See all CMSS1 Antibodies
CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))

Reactivity

  • 16
  • 12
  • 12
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 16
Rabbit

Clonality

  • 16
Polyclonal

Conjugate

  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CMSS1 antibody is conjugated to Cy5.5

Application

  • 16
  • 3
Western Blotting (WB)
  • Cross-Reactivity

    Human

    Predicted Reactivity

    Mouse,Rat,Horse

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human C3orf26

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200

    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

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))

    Alternative Name

    C3orf26

    Background

    Synonyms: C3orf26, CC026_HUMAN, MGC4308, Uncharacterized protein C3orf26.

    Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf26 gene product has been provisionally designated C3orf26 pending further characterization.

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