产品: N Cadherin 抗体
货号: AF4039
描述: Rabbit polyclonal antibody to N Cadherin
应用: WB IHC IF/ICC
反应: Human, Mouse, Rat
预测: Pig, Zebrafish, Bovine, Horse, Sheep, Rabbit, Dog, Chicken, Xenopus
分子量: 140kd; 100kD(Calculated).
蛋白号: P19022
RRID: AB_2835344

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 200ul RMB¥ 3000 现货

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产品描述

来源:
Rabbit
应用:
WB 1:500-1:1000, IHC 1:50-200, IF/ICC 1:200
*The optimal dilutions should be determined by the end user.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human,Mouse,Rat
预测:
Pig(100%), Zebrafish(100%), Bovine(100%), Horse(100%), Sheep(100%), Rabbit(100%), Dog(100%), Chicken(100%), Xenopus(100%)
克隆:
Polyclonal
特异性:
N Cadherin Antibody detects endogenous levels of total N Cadherin.
RRID:
AB_2835344
引用格式: Affinity Biosciences Cat# AF4039, RRID:AB_2835344.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

CADH2_HUMAN; Cadherin 2; Cadherin 2 N cadherin neuronal; Cadherin 2 type 1; Cadherin 2 type 1 N cadherin neuronal; Cadherin 2, type 1, N-cadherin (neuronal); Cadherin-2; Cadherin2; Calcium dependent adhesion protein neuronal; CD325; CD325 antigen; CDH2; CDHN; CDw325; CDw325 antigen; N cadherin 1; N-cadherin; NCAD; Neural cadherin; OTTHUMP00000066304; OTTHUMP00000067378;

抗原和靶标

免疫原:
Uniprot:
基因/基因ID:
描述:
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. CDH2 may be involved in neuronal recognition mechanism. In hippocampal neurons, may regulate dendritic spine density
序列:
MCRIAGALRTLLPLLAALLQASVEASGEIALCKTGFPEDVYSAVLSKDVHEGQPLLNVKFSNCNGKRKVQYESSEPADFKVDEDGMVYAVRSFPLSSEHAKFLIYAQDKETQEKWQVAVKLSLKPTLTEESVKESAEVEEIVFPRQFSKHSGHLQRQKRDWVIPPINLPENSRGPFPQELVRIRSDRDKNLSLRYSVTGPGADQPPTGIFIINPISGQLSVTKPLDREQIARFHLRAHAVDINGNQVENPIDIVINVIDMNDNRPEFLHQVWNGTVPEGSKPGTYVMTVTAIDADDPNALNGMLRYRIVSQAPSTPSPNMFTINNETGDIITVAAGLDREKVQQYTLIIQATDMEGNPTYGLSNTATAVITVTDVNDNPPEFTAMTFYGEVPENRVDIIVANLTVTDKDQPHTPAWNAVYRISGGDPTGRFAIQTDPNSNDGLVTVVKPIDFETNRMFVLTVAAENQVPLAKGIQHPPQSTATVSVTVIDVNENPYFAPNPKIIRQEEGLHAGTMLTTFTAQDPDRYMQQNIRYTKLSDPANWLKIDPVNGQITTIAVLDRESPNVKNNIYNATFLASDNGIPPMSGTGTLQIYLLDINDNAPQVLPQEAETCETPDPNSINITALDYDIDPNAGPFAFDLPLSPVTIKRNWTITRLNGDFAQLNLKIKFLEAGIYEVPIIITDSGNPPKSNISILRVKVCQCDSNGDCTDVDRIVGAGLGTGAIIAILLCIIILLILVLMFVVWMKRRDKERQAKQLLIDPEDDVRDNILKYDEEGGGEEDQDYDLSQLQQPDTVEPDAIKPVGIRRMDERPIHAEPQYPVRSAAPHPGDIGDFINEGLKAADNDPTAPPYDSLLVFDYEGSGSTAGSLSSLNSSSSGGEQDYDYLNDWGPRFKKLADMYGGGDD

种属预测

种属预测:

score>80的预测可信度较高,可尝试用于WB检测。*预测模型主要基于免疫原序列比对,结果仅作参考,不作为质保凭据。

Species
Results
Score
Pig
100
Horse
100
Bovine
100
Sheep
100
Dog
100
Xenopus
100
Zebrafish
100
Chicken
100
Rabbit
100
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

翻译修饰 - P19022 作为底物

Site PTM Type Enzyme
S61 Phosphorylation
S96 Phosphorylation
S135 Phosphorylation
N273 N-Glycosylation
N402 N-Glycosylation
K448 Ubiquitination
T454 Phosphorylation
Y496 Phosphorylation
K536 Ubiquitination
N572 N-Glycosylation
K667 Ubiquitination
T683 Phosphorylation
S685 Phosphorylation
N692 N-Glycosylation
K756 Ubiquitination
K772 Ubiquitination
Y773 Phosphorylation
Y785 Phosphorylation
S788 Phosphorylation
K802 Ubiquitination
Y820 Phosphorylation P12931 (SRC)
S824 Phosphorylation
Y852 Phosphorylation P12931 (SRC)
Y860 Phosphorylation P12931 (SRC)
Y884 Phosphorylation P12931 (SRC)
Y886 Phosphorylation P12931 (SRC)

研究背景

功能:

Calcium-dependent cell adhesion protein; preferentially mediates homotypic cell-cell adhesion by dimerization with a CDH2 chain from another cell. Cadherins may thus contribute to the sorting of heterogeneous cell types. Acts as a regulator of neural stem cells quiescence by mediating anchorage of neural stem cells to ependymocytes in the adult subependymal zone: upon cleavage by MMP24, CDH2-mediated anchorage is affected, leading to modulate neural stem cell quiescence. CDH2 may be involved in neuronal recognition mechanism. In hippocampal neurons, may regulate dendritic spine density.

翻译修饰:

Cleaved by MMP24. Ectodomain cleavage leads to the generation of a soluble 90 kDa amino-terminal soluble fragment and a 45 kDa membrane-bound carboxy-terminal fragment 1 (CTF1), which is further cleaved by gamma-secretase into a 35 kDa. Cleavage in neural stem cells by MMP24 affects CDH2-mediated anchorage of neural stem cells to ependymocytes in the adult subependymal zone, leading to modulate neural stem cell quiescence (By similarity).

May be phosphorylated by OBSCN.

细胞定位:

Cell membrane>Single-pass type I membrane protein. Cell membrane>Sarcolemma. Cell junction. Cell surface.
Note: Colocalizes with TMEM65 at the intercalated disk in cardiomyocytes. Colocalizes with OBSCN at the intercalated disk and at sarcolemma in cardiomyocytes.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
亚基结构:

Homodimer (via extracellular region). Can also form heterodimers with other cadherins (via extracellular region). Dimerization occurs in trans, i.e. with a cadherin chain from another cell (By similarity). Interacts with CDCP1. Interacts with PCDH8; this complex may also include TAOK2 (By similarity). The interaction with PCDH8 may lead to internalization through TAOK2/p38 MAPK pathway (By similarity). Identified in a complex containing FGFR4, NCAM1, CDH2, PLCG1, FRS2, SRC, SHC1, GAP43 and CTTN. May interact with OBSCN (via protein kinase domain 2) (By similarity).

蛋白家族:

Three calcium ions are usually bound at the interface of each cadherin domain and rigidify the connections, imparting a strong curvature to the full-length ectodomain. Calcium-binding sites are occupied sequentially in the order of site 3, then site 2 and site 1.

研究领域

· Environmental Information Processing > Signaling molecules and interaction > Cell adhesion molecules (CAMs).   (View pathway)

· Human Diseases > Cardiovascular diseases > Arrhythmogenic right ventricular cardiomyopathy (ARVC).

文献引用

1). METTL13 Mediates the Translation of Snail in Head and Neck Squamous Cell Carcinoma. International Journal of Oral Science, 2020 (PubMed: 34381012) [IF=14.9]

2). d-Borneol enhances cisplatin sensitivity via autophagy dependent EMT signaling and NCOA4-mediated ferritinophagy. PHYTOMEDICINE, 2022 (PubMed: 36030746) [IF=7.9]

3). Huaier polysaccharides suppress triple-negative breast cancer metastasis and epithelial-mesenchymal transition by inducing autophagic degradation of Snail. Cell and Bioscience, 2021 (PubMed: 34481526) [IF=7.5]

Application: WB    Species: human    Sample: breast cancer cells

Fig. 1| PS-T inhibits invasion, migration and EMT in breast cancer cells in vitro and in vivo. d 4 T-1 and MDA-MB-231 cells are treated with 5 μg/mL PS-T for 24 h. The levels of each EMT marker are quantifed using the NIH ImageJ software. (mean ± SD, *P < 0.05 and **P < 0.01)

Application: WB    Species: Human    Sample: breast cancer cells

Fig. 1 PS-T inhibits invasion, migration and EMT in breast cancer cells in vitro and in vivo. a The invasiveness of 4 T-1 and MDA-MB-231 cells after treatment with PS-T at 5 μg/mL for 12 h is evaluated using Transwell invasion assays at 24 h (mean  ±  SD, ***P  <  0.001). b Migratory ability of 4 T-1 and MDA-MB-231 cells after treatment with PS-T at different concentrations is evaluated using scratch assays at different time points (mean  ±  SD, **P  <  0.01, ***P  <  0.001). c Mice are treated with normal saline (control), 25 μg/g or 100 μg/g PS-T by oral gavage every other day for 21 days (mean  ±  SD, *P  <  0.05, **P  <  0.01, scale bars: 100 μm). d 4 T-1 and MDA-MB-231 cells are treated with 5 μg/mL PS-T for 24 h. The levels of each EMT marker are quantified using the NIH ImageJ software. (mean  ±  SD, *P  <  0.05 and **P  <  0.01)

4). TRIP13 interference inhibits the proliferation and metastasis of thyroid cancer cells through regulating TTC5/p53 pathway and epithelial-mesenchymal transition related genes expression. BIOMEDICINE & PHARMACOTHERAPY, 2019 (PubMed: 31648166) [IF=7.5]

5). Molecular mechanism of albumin in suppressing invasion and metastasis of hepatocellular carcinoma. LIVER INTERNATIONAL, 2022 (PubMed: 34854209) [IF=6.7]

Application: WB    Species: Human    Sample: HepG2 and Huh7 cells

FIGURE 7 A, Representative images of the western blot results for uPAR, MMP2 and MMP9 in ALB knockdown HepG2 and Huh7 cells; B, Zymography analysis illustrates MMP2 and MMP9 activity in ALB knockdown HepG2 and Huh7 cells; C, Quantitative analysis results and representative images of the western blot results for the EMT‐associated markers, E‐cadherin, N‐cadherin, vimentin, Snail and Twist by western blot in ALB knockdown HepG2 and Huh7 cells; D, Quantification shows a significantly higher uPAR in HCC group with ALB <3.5 g/dL compared to ALB ≥3.5 g/dL (*P < .05); E, Scatterplot showing the correlation between plasma levels of ALB and uPAR. The vertical position represents the expression levels of uPAR (lg pg/mL)

6). Tspan5 promotes epithelial–mesenchymal transition and tumour metastasis of hepatocellular carcinoma by activating Notch signalling. Molecular Oncology, 2021 (PubMed: 33955149) [IF=6.6]

Application: WB    Species: Human    Sample: HCC cells

Fig. 3 Tspan5 promotes EMT of HCC cells. (A) Tspan5 triggers the rearrangement of actin cytoskeleton. Stress fibres and actin filaments were visualized by Rhodamine-phalloidin staining (red) in HCC cells transduced with lentivirus containing Tspan5/shTspan5-encoding vector or empty/scramble RNA vector (Control/shControl). Nuclei were stained with DAPI (blue). Upregulation of Tspan5 significantly increased F-actin expression (red) and actin stress fibres throughout the Tspan5-upregulating cells compared with the control cells in which the actin bundles were predominantly localized underneath cell membranes. 400× magnification, scale bar: 10 μm. Mean ± SD, n = 3, Student's t-test; *P < 0.05, **P < 0.01. (B) Western blotting showing regulation of the expression of EMT markers, E-cadherin, N-cadherin, vimentin and Snail by Tspan5. GAPDH was used as a protein loading control. Numbers indicating relative protein ratio measured by Image J software and normalized to GAPDH. Vimentin was undetectable in MHCC97L cells. (C) Representative IF images showing regulation of the expressions of E-cadherin and vimentin by Tspan5. 630× magnifications, scale bar: 10 μm. Quantification of the protein expression was performed by Zeiss zen microscope software. Mean ± SD, n = 9, Student's t-test; **P < 0.01. (D) Representative IHC images of Tspan5, E-cadherin and vimentin expressions in xenograft sections of metastatic foci in mouse lungs. 600× magnifications, scale bar: 50 μm. Mean ± SD,

Application: IF/ICC    Species: Human    Sample: HCC cells

Fig. 3 Tspan5 promotes EMT of HCC cells. (A) Tspan5 triggers the rearrangement of actin cytoskeleton. Stress fibres and actin filaments were visualized by Rhodamine-phalloidin staining (red) in HCC cells transduced with lentivirus containing Tspan5/shTspan5-encoding vector or empty/scramble RNA vector (Control/shControl). Nuclei were stained with DAPI (blue). Upregulation of Tspan5 significantly increased F-actin expression (red) and actin stress fibres throughout the Tspan5-upregulating cells compared with the control cells in which the actin bundles were predominantly localized underneath cell membranes. 400× magnification, scale bar: 10 μm. Mean ± SD, n = 3, Student's t-test; *P < 0.05, **P < 0.01. (B) Western blotting showing regulation of the expression of EMT markers, E-cadherin, N-cadherin, vimentin and Snail by Tspan5. GAPDH was used as a protein loading control. Numbers indicating relative protein ratio measured by Image J software and normalized to GAPDH. Vimentin was undetectable in MHCC97L cells. (C) Representative IF images showing regulation of the expressions of E-cadherin and vimentin by Tspan5. 630× magnifications, scale bar: 10 μm. Quantification of the protein expression was performed by Zeiss zen microscope software. Mean ± SD, n = 9, Student's t-test; **P < 0.01. (D) Representative IHC images of Tspan5, E-cadherin and vimentin expressions in xenograft sections of metastatic foci in mouse lungs. 600× magnifications, scale bar: 50 μm. Mean ± SD,

7). Polydopamine/carboxylic graphene oxide-composited polypyrrole films for promoting adhesion and alignment of Schwann cells. Colloids and surfaces-B, Biointerfaces, 2020 (PubMed: 32203860) [IF=5.8]

Application: WB    Species:    Sample: RSCs

Fig. 3.| Cell images of immunofluorescence staining for (a) N-cadherin expression, phalloidin, (b) GFAP, (c) S100 and DAPI, and scale bar is 50 μm. (d) WB assay for Vinculin, Ncadherin, P75 and GFAP proteins and (e) their semi-quantitative comparison. & shows p<0.05, compared with control; # shows p<0.05, compared with PPy-PLLA; Δ shows p<0.05, compared with CGO/PPy-PLLA.

Application: IF/ICC    Species:    Sample: RSCs

Fig. 3.| Cell images of immunofluorescence staining for (a) N-cadherin expression, phalloidin, (b) GFAP, (c) S100 and DAPI, and scale bar is 50 μm. (d) WB assay for Vinculin, Ncadherin, P75 and GFAP proteins and (e) their semi-quantitative comparison. & shows p<0.05, compared with control; # shows p<0.05, compared with PPy-PLLA; Δ shows p<0.05, compared with CGO/PPy-PLLA.

8). Entrectinib ameliorates bleomycin-induced pulmonary fibrosis in mice by inhibiting TGF-β1 signaling pathway. International Immunopharmacology, 2022 (PubMed: 36375321) [IF=5.6]

9). NUDCD1 knockdown inhibits the proliferation, migration, and invasion of pancreatic cancer via the EMT process. Aging (Albany NY), 2021 (PubMed: 34325402) [IF=5.2]

Application: WB    Species: human    Sample: PANC-1 cells

Figure 5.| NUDCD1 knockdown inhibited the EMT process in PC cells. (A–D) NUDCD1 knockdown decreased the expression of Ncadherin and vimentin and upregulated the expression of E-cadherin in PANC-1 cells.

Application: WB    Species: Human    Sample: PANC-1 cells

Figure 5 NUDCD1 knockdown inhibited the EMT process in PC cells. (A–D) NUDCD1 knockdown decreased the expression of N-cadherin and vimentin and upregulated the expression of E-cadherin in PANC-1 cells. (E–H) NUDCD1 knockdown decreased the expression of N-cadherin and vimentin, and upregulated the expression of E-cadherin in Patu8988 cells. ***p<0.001, ****p<0.0001.

10). Neuron specific enolase promotes tumor metastasis by activating the Wnt/β-catenin pathway in small cell lung cancer. Translational Oncology, 2021 (PubMed: 33618068) [IF=5.0]

Application: WB    Species: Human    Sample: sclc cells

Fig. 3. NSE induced EMT in SCLC cells. (A, B) NSE overexpression promoted the EMT process of SCLC. (A) Western blot assay was performed to measure the protein expression levels of the EMT-related markers (Snail, N-cadherin and E-cadherin). (B) qRT-PCR was performed to measure the mRNA expression levels of the EMT markers. (C, D) NSE knockdown represses the EMT process of SCLC. Protein levels (C) and mRNA levels (D) of EMT-related markers were measured using western blot or qRT-PCR, respectively. These results were repeated of three independent experiments.

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