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MANSC1 antibody (AA 21-337)

The Rabbit Polyclonal anti-MANSC1 antibody is suitable to detect MANSC1 in samples from Human. It has been validated for WB and ELISA.
Catalog No. ABIN7872165
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for MANSC1 antibody (AA 21-337) (ABIN7872165)

Target

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

Reactivity

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  • 2
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  • 1
  • 1
  • 1
Human

Host

  • 38
Rabbit

Clonality

  • 38
Polyclonal

Conjugate

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  • 1
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This MANSC1 antibody is un-conjugated

Application

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  • 14
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  • 4
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  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

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    AA 21-337

    Purpose

    MANSC1 Antibody / MANSC domain-containing protein 1

    Purification

    Antigen affinity purified

    Immunogen

    An E.coli-derived human recombinant protein (amino acids L21-N337) was used as the immunogen for the MANSC1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the MANSC1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the MANSC1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 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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