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CMSS1 antibody (AA 101-200) (Biotin)

This anti-CMSS1 antibody is a Rabbit Polyclonal antibody detecting CMSS1 in WB and ELISA. Suitable for Human.
Catalog No. ABIN1700223

Quick Overview for CMSS1 antibody (AA 101-200) (Biotin) (ABIN1700223)

Target

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

Reactivity

  • 16
  • 13
  • 13
  • 1
  • 1
  • 1
Human

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 Biotin

Application

Western Blotting (WB), ELISA
  • Binding Specificity

    • 2
    • 2
    AA 101-200

    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

    WB 1:300-5000

    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

    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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