Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

MANSC1 antibody

This Rabbit Polyclonal antibody specifically detects MANSC1 in ELISA and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN7247171

Quick Overview for MANSC1 antibody (ABIN7247171)

Target

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

Reactivity

  • 23
  • 16
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 37
  • 1
Rabbit

Clonality

  • 37
  • 1
Polyclonal

Conjugate

  • 12
  • 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

  • 31
  • 13
  • 13
  • 13
  • 5
  • 4
  • 3
  • 3
  • 2
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
You are here:
Chat with us!