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MANSC1 antibody

This Rabbit Polyclonal antibody specifically detects MANSC1 in ELISA and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN7247171
-15% Promotion 2026
$457.98
$538.80
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Quick Overview for MANSC1 antibody (ABIN7247171)

Target

See all MANSC1 Antibodies
MANSC1 (MANSC Domain Containing 1 (MANSC1))

Reactivity

  • 21
  • 16
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 36
Rabbit

Clonality

  • 36
Polyclonal

Conjugate

  • 10
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MANSC1 antibody is un-conjugated

Application

  • 29
  • 13
  • 13
  • 13
  • 4
  • 3
  • 3
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human MANSC1

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.8 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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. Avoid freeze / thaw cycles.
  • Target

    MANSC1 (MANSC Domain Containing 1 (MANSC1))

    Alternative Name

    MANSC1

    Background

    MANSC1 (MANSC domain-containing protein 1), also known as LOH12CR3 (Loss of heterozygosity 12 chromosomal region 3 protein), is a 414 amino acid single-pass membrane protein. Expressed throughout the body, MANSC1 contains one MANSC domain and is encoded by a gene that is located on chromosome 12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.

    UniProt

    Q9H8J5
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