IHC

E-Cadherin (ABT270) Mouse mAb (Ready to Use)

-YM6127R

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Catalog: YM6127R
Size
Price
Status
Qty.
10mL
$150.00
3 weeks

0

6mL
$120.00
3 weeks

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3mL
$70.00
3 weeks

0

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Main Information
Target

E-cadherin

Host Species

Mouse

Reactivity

Human

Applications

IHC

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
Ready to use for IHC
Formulation
The prediluted ready-to-use antibody is diluted in phosphate buffer saline containing stabilizing protein and 0.05% Proclin 300
Specificity
The antibody can specifically recognize E-cadherin protein.
Purification
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
Storage
2°C to 8°C/1 year,Ship by ice bag
Modification
Unmodified
Clonality
Monoclonal
Clone Number
ABT270
Isotype
Mouse IgG2b/Kappa
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human E-Cadherin AA range: 700-800
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Specificity:
The antibody can specifically recognize E-cadherin protein.
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Gene Name:
CDH1 CDHE UVO
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Protein Name:
Cadherin-1 (CAM 120/80) (Epithelial cadherin) (E-cadherin) (Uvomorulin) (CD antigen CD324) [Cleaved into: E-Cad/CTF1; E-Cad/CTF2; E-Cad/CTF3]
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Database Link:
Organism Gene ID SwissProt
Human 999; P12830;
Background:
This gene encodes a classical cadherin of the cadherin superfamily. Alternative splicing results in multiple transcript variants , at least one of which encodes a preproprotein that is proteolytically processed to generate the mature glycoprotein. This calcium-dependent cell-cell adhesion protein is comprised of five extracellular cadherin repeats , a transmembrane region and a highly conserved cytoplasmic tail. Mutations in this gene are correlated with gastric , breast , colorectal , thyroid and ovarian cancer. Loss of function of this gene is thought to contribute to cancer progression by increasing proliferation , invasion , and/or metastasis. The ectodomain of this protein mediates bacterial adhesion to mammalian cells and the cytoplasmic domain is required for internalization. This gene is present in a gene cluster with other members of the cadherin family on chromosome 16. [provided by RefSeq , Nov 2015] ,
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Function:
Disease:Defects in CDH1 are a cause of gastric cancer [MIM:137215]; also known as hereditary familial diffuse gastric cancer (HDGC) . ,Disease:Defects in CDH1 are a cause of susceptibility to endometrial cancer [MIM:608089]. ,Disease:Defects in CDH1 are associated with ovarian cancer [MIM:167000]. Ovarian cancer is the leading cause of death from gynecologic malignancy. It is characterized by advanced presentation with loco-regional dissemination in the peritoneal cavity and the rare incidence of visceral metastases. These typical features relate to the biology of the disease , which is a principal determinant of outcome. ,Disease:Defects in CDH1 are involved in dysfunction of the cell-cell adhesion system , triggering cancer invasion (gastric , breast , ovary , endometrium and thyroid) and metastasis. ,Function:Cadherins are calcium dependent cell adhesion proteins. ,Function:Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. CDH1 is involved in mechanisms regulating cell-cell adhesions , mobility and proliferation of epithelial cells. Has a potent invasive suppressor role. It is a ligand for integrin alpha-E/beta-7. ,Function:E-Cad/CTF2 promotes non-amyloidogenic degradation of Abeta precursors. Has a strong inhibitory effect on APP C99 and C83 production. ,online information:E-cadherin entry ,PTM:During apoptosis or with calcium influx , cleaved by a membrane-bound metalloproteinase (ADAM10) , PS1/gamma-secretase and caspase-3 to produce fragments of about 38 kDa (E-CAD/CTF1) , 33 kDa (E-CAD/CTF2) and 29 kDa (E-CAD/CTF3) , respectively. Processing by the metalloproteinase , induced by calcium influx , causes disruption of cell-cell adhesion and the subsequent release of beta-catenin into the cytoplasm. The residual membrane-tethered cleavage product is rapidly degraded via an intracellular proteolytic pathway. Cleavage by caspase-3 releases the cytoplasmic tail resulting in disintegration of the actin microfilament system. The gamma-secretase-mediated cleavage promotes disaaaembly of adherens junctions. ,similarity:Contains 5 cadherin domains. ,subcellular location:Colocalizes with DLGAP5 at sites of cell-cell contact in intestinal epithelial cells. Anchored to actin microfilaments through association with alpha- , beta- and gamma-catenin. Sequential proteolysis induced by apoptosis or calcium influx , results in translocation from sites of cell-cell contact to the cytoplasm. ,subunit:Homodimer; disulfide-linked. Interacts directly , via the cytoplasmic domain , with CTNNB1 or JUP to form the PSEN1/cadherin/catenin adhesion complex which connects to the actin skeleton through the actin binding of alpha-catenin. Interaction with PSEN1 , cleaves CDH1 resulting in the disassociation of cadherin-based adherens junctions (CAJs) . Interacts with AJAP1 , CTNND1 and DLGAP5. ,tissue specificity:Non-neural epithelial tissues. ,
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Cellular Localization:
Membranous
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Tissue Expression:
Research Areas:
>>Rap1 signaling pathway ;
>>Apelin signaling pathway ;
>>Hippo signaling pathway ;
>>Cell adhesion molecules ;
>>Adherens junction ;
>>Bacterial invasion of epithelial cells ;
>>Pathways in cancer ;
>>Endometrial cancer ;
>>Thyroid cancer ;
>>Melanoma ;
>>Bladder cancer ;
>>Gastric cancer
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Catalog: YM6127R
Size
Price
Status
Qty.
10mL
$150.00
3 weeks

0

6mL
$120.00
3 weeks

0

3mL
$70.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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