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

Sonic Hedgehog antibody

SHH Reactivity: Human ELISA Host: Mouse Monoclonal 8G3 unconjugated
Catalog No. ABIN969395
  • Target See all Sonic Hedgehog (SHH) Antibodies
    Sonic Hedgehog (SHH)
    Reactivity
    • 65
    • 50
    • 37
    • 17
    • 10
    • 6
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 73
    • 11
    • 8
    • 1
    • 1
    Mouse
    Clonality
    • 68
    • 26
    Monoclonal
    Conjugate
    • 51
    • 8
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Sonic Hedgehog antibody is un-conjugated
    Application
    • 69
    • 27
    • 23
    • 14
    • 13
    • 11
    • 9
    • 7
    • 6
    • 6
    • 5
    • 4
    • 3
    • 1
    ELISA
    Purpose
    SHH Antibody
    Purification
    Ascitic fluid
    Immunogen
    Purified recombinant fragment of human SHH expressed in E. Coli.
    Clone
    8G3
    Isotype
    IgG1
    Top Product
    Discover our top product SHH Primary Antibody
  • Application Notes
    ELISA: 1/10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Ascitic fluid containing 0.03 % sodium azide.
    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
    4 °C,-20 °C
    Storage Comment
    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Dia, Mejia: "Lunasin promotes apoptosis in human colon cancer cells by mitochondrial pathway activation and induction of nuclear clusterin expression." in: Cancer letters, Vol. 295, Issue 1, pp. 44-53, (2010) (PubMed).

    Dierker, Dreier, Migone, Hamer, Grobe: "Heparan sulfate and transglutaminase activity are required for the formation of covalently cross-linked hedgehog oligomers." in: The Journal of biological chemistry, Vol. 284, Issue 47, pp. 32562-71, (2009) (PubMed).

    Bailey, Mohr, Hollingsworth: "Sonic hedgehog paracrine signaling regulates metastasis and lymphangiogenesis in pancreatic cancer." in: Oncogene, Vol. 28, Issue 40, pp. 3513-25, (2009) (PubMed).

  • Target
    Sonic Hedgehog (SHH)
    Alternative Name
    SHH (SHH Products)
    Synonyms
    HHG1 antibody, HLP3 antibody, HPE3 antibody, MCOPCB5 antibody, SMMCI antibody, TPT antibody, TPTPS antibody, 9530036O11Rik antibody, Dsh antibody, Hhg1 antibody, Hx antibody, Hxl3 antibody, M100081 antibody, fc83d08 antibody, shh antibody, syu antibody, vhh-1 antibody, vhh1 antibody, wu:fc83d08 antibody, Xhh antibody, hedgehog antibody, xshh antibody, SHH antibody, twh antibody, twhh antibody, sonic hedgehog antibody, sonic hedgehog a antibody, sonic hedgehog L homeolog antibody, sonic hedgehog protein A antibody, sonic hedgehog b antibody, SHH antibody, Shh antibody, shha antibody, shh.L antibody, shh antibody, shhb antibody
    Background

    Description: This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved, the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right and left hemispheres. HPE is manifested by facial deformities. It is also thought that mutations in this gene or in its signalling pathway may be responsible for VACTERL syndrome, which is characterized by vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, radial and renal dysplasia, cardiac anomalies, and limb abnormalities. Additionally, mutations in a long range enhancer located approximately 1 megabase upstream of this gene disrupt limb patterning and can result in preaxial polydactyly.

    Aliases: TPT, HHG1, HLP3, HPE3, SMMCI, TPTPS, MCOPCB5, SHH

    Molecular Weight
    49.6kDa
    Gene ID
    6469
    HGNC
    6469
    UniProt
    Q15465
    Pathways
    Hedgehog Signaling, Dopaminergic Neurogenesis, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development
You are here:
Support