收藏本站
热门搜索: A3500  E1910  A1360  25200056  dmem  

Anti-Sonic Hedgehog (C-product), clone EP1190Y, Rabbit Monoclonal

  • 产品编号:merck-m-04-971      品牌:millipore       原厂货号:04-971
  • 产品分类:抗体 > 一抗 > 蛋白特异性一抗
  • 应用分类:
 
包装:
运保温度: -20ºC
到货周期: 登录后查看
标准价: ¥客户可见
会员价: ¥客户可见
积分: 客户可见
 
登录之后可加入购物车购买,请您 
对比 收藏

运费与支付说明:

1.含干冰类产品有运费;

2. 必须现金付款或有信用额度的会员才可以直接发货,否则需要等待现金付款信息。

描述:

Key Spec Table

Species Reactivity Key Applications Host Format Antibody Type
H WB, IP, FC, IH(P) Rb Purified Monoclonal Antibody

Description 
Catalogue Number 04-971
Description Anti-Sonic Hedgehog (C-product) Antibody, clone EP1190Y, Rabbit | 04-971
Alternate Names
  • sonic hedgehog homolog (Drosophila)
  • sonic hedgehog
  • sonic hedgehog (Drosophila) homolog
Background Information Sonic Hedgehog Protein (SHH, VHH-1) belongs to hedgehog protein family which includes Indian Hh, and Desert Hh. Hh family is involved in the cell fate and patterning during embryonic development, homeostasis, and adult tissue renewal. Similar to other member in the family, SHH binds to the patched (PTC) cell surface receptor, releasing the signal transducer Smoothened (Smo) to transmit the Hh signal into the cell and activate transcription of the target gene. Precursor SHH is autocatlytically cleaved into two subunits, N-terminal and C-terminal products. Soluble N-terminal product is involved in the signaling activity, while C-product displays an autoproteolysis activity on the precursor and a cholesterol transferase activity on the N-terminal product. C-terminal product attaches a cholesterol moiety to the N-terminal product, preventing N-terminal product diffusion within the developing embryo. A defect in SHH has been linked in holoprosencephaly type 3 (HPE3), in which developing forebrain fails to separate into right and left hemispheres, and ocular coloboma.

Product Information 
Format Purified
Control
  • Fetal liver membrane, human kidney tissue.
Presentation Rabbit monoclonal IgG in buffer containing 50 mM Tris-Glycine (pH7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA.

Applications 
Application Please note that this product will not be available for sale after March 15, 2015. Please select one of the other antibodies against this target.
Key Applications
  • Western Blotting
  • Immunoprecipitation
  • Flow Cytometry
  • Immunohistochemistry (Paraffin)
Application Notes Flow Cytometry: A 1:40 dilution of a previous lot was used in flow cytometry.

Immunoprecipitation: A 1:70 dilution of a previous lot was used in immunoprecipitation.

Immunohistochemistry (paraffin): A 1:100 dilution of a previous lot was used in immunohistochemsitry.

Biological Information 
Immunogen A synthetic peptide corresponding to residues within c-product subunit of human SHH protein was used as an immunogen.
Epitope C-product
Clone EP1190Y
Host Rabbit
Specificity This antibody is specific for both full length (50 kDa) and c-product subunit (27 kDa) of human SHH protein. Sonic hedgehog protein C-product is secreted and can be found in the extracellular space.
Isotype IgG
Species Reactivity Human
Species Reactivity Note Human
Antibody Type Monoclonal Antibody
Entrez Gene Number
Gene Symbol
  • HHG-1
  • TPTPS
  • TPT
  • SMMCI
  • MCOPCB5
  • HPE3
  • HLP3
  • HHG1
UniProt Number
UniProt Summary FUNCTION: Binds to the patched (PTC) receptor, which functions in association with smoothened (SMO), to activate the transcription of target genes. In the absence of SHH, PTC represses the constitutive signaling activity of SMO. Also regulates another target, the gli oncogene. Intercellular signal essential for a variety of patterning events during development: signal produced by the notochord that induces ventral cell fate in the neural tube and somites, and the polarizing signal for patterning of the anterior-posterior axis of the developing limb bud. Displays both floor plate- and motor neuron-inducing activity. The threshold concentration of N-product required for motor neuron induction is 5-fold lower than that required for floor plate induction By similarity.

SUBUNIT STRUCTURE: Interacts with HHATL/GUP1 which negatively regulates HHAT-mediated palmitoylation of the SHH N-terminus. N-product is active as a multimer By similarity.

SUBCELLULAR LOCATION: Sonic hedgehog protein C-product: Secreted › extracellular spaceBy similarity. Note= The C-terminal peptide diffuses from the cell By similarity.

Sonic hedgehog protein N-product: Cell membrane; Lipid-anchorBy similarity. Note= The N-product either remains associated with lipid rafts at the cell surface, or forms freely diffusible active multimers with its hydrophobic lipid-modified N- and C-termini buried inside By similarity.

TISSUE SPECIFICITY: Expressed in fetal intestine, liver, lung, and kidney. Not expressed in adult tissues.

PTM: The C-terminal domain displays an autoproteolysis activity and a cholesterol transferase activity. Both activities result in the cleavage of the full-length protein and covalent attachment of a cholesterol moiety to the C-terminal of the newly generated N-terminal fragment (N-product). The N-product is the active species in both local and long-range signaling, whereas the C-product has no signaling activity.

Cholesterylation is required for N-product targeting to lipid rafts and multimerization By similarity.

N-palmitoylation of Cys-24 by HHAT is required for N-product multimerization and full activity By similarity.

INVOLVEMENT IN DISEASE: Defects in SHH are the cause of microphthalmia isolated with coloboma type 5 (MCOPCB5) [MIM:611638]. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Ocular abnormalities like opacities of the cornea and lens, scaring of the retina and choroid, cataract and other abnormalities like cataract may also be present. Ocular colobomas are a set of malformations resulting from abnormal morphogenesis of the optic cup and stalk, and the fusion of the fetal fissure (optic fissure). 

Defects in SHH are the cause of holoprosencephaly type 3 (HPE3) [MIM:142945]. Holoprosencephaly (HPE) [MIM:236100] is the most common structural anomaly of the brain, in which the developing forebrain fails to correctly separate into right and left hemispheres. Holoprosencephaly is genetically heterogeneous and associated with several distinct facies and phenotypic variability. The majority of HPE3 cases are apparently sporadic, although clear exemples of autosomal dominant inheritance have been described. Interestingly, up to 30% of obligate carriers of HPE3 gene in autosomal dominant pedigrees are clinically unaffected. 

Defects in SHH are a cause of solitary median maxillary central incisor (SMMCI) [MIM:147250]. SMMCI is a rare dental anomaly characterized by the congenital absence of one maxillary central incisor. 

Defects in SHH are the cause of triphalangeal thumb-polysyndactyly syndrome (TPTPS) [MIM:174500]. TPTPS is an autosomal dominant syndrome characterized by a wide spectrum of pre- and post-axial abnormalities due to altered SHH expression pattern during limb development. TPTPS mutations have been mapped to the 7q36 locus in the LMBR1 gene which contains in its intron 5 a long-range cis-regulatory element of SHH expression. 

SEQUENCE SIMILARITIES: Belongs to the hedgehog family.

MASS SPECTROMETRY: Molecular weight is 19.560 Da from positions 24 - 197. Determined by ESI. Soluble N-product, purified from insect cells. 

Molecular weight is 20.167 Da from positions 24 - 197. Determined by ESI. Membrane-bound N-product, purified from insect cells. 
 

Product Usage Statements 
Quality Assurance Evaluated by Western Blotting on fetal liver membrane lysate.

Western Blotting Analysis: 1:2,000 dilution of this antibody detected full length and c-product subunit of sonic hedgehog in fetal liver membrane lysate.
Usage Statement
  • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Storage and Shipping Information 
Storage Conditions Stable for 1 year at -20ºC from date of receipt.
Handling Recommendations: Upon receipt, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance. Note: Variability in freezer temperatures below -20°C may cause glycerolcontaining solutions to become frozen during storage.

Packaging Information 
Material Size 100 µL

 


相关图片

说明书

参考文献

本产品可用于的实验

购此产品的人还购买了
最近浏览产品

京ICP备15036693号-2    京公网安备11010802025653    版权所有:北京逸优科技有限公司       1.7

 纠 错