PDPN Recombinant Monoclonal Antibody

中文名稱：

PDPN重組抗體
貨號(hào)：

CSB-RA017739MA1HU
規(guī)格：

￥1320
圖片：
Western Blot
Positive WB detected in: PC-3 whole cell lysate, SY5Y whole cell lysate, U251 whole cell lysate, HepG2 whole cell lysate
All lanes: PDPN antibody at 1:1000
Secondary
Goat polyclonal to mouse IgG at 1/50000 dilution
Predicted band size: 17 kDa
Observed band size: 17 kDa

IHC image of CSB-RA017739MA1HU diluted at 1:300 and staining in paraffin-embedded human colorectal cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-Mouse IgG labeled by HRP and visualized using 0.05% DAB.

IHC image of CSB-RA017739MA1HU diluted at 1:300 and staining in paraffin-embedded human placenta tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-Mouse IgG labeled by HRP and visualized using 0.05% DAB.

Overlay Peak curve showing 293 cells stained with CSB-RA017739MA1HU (red line) at 1:100. The cells were fixed in 4% formaldehyde (15min) and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10⁶cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG(H+L) at 1/200 dilution for 35 min at 4°C. Isotype control antibody (green line) was mouse IgG1 (1μg/1*10⁶cells) used under the same conditions. Acquisition of >10,026 events was performed.
其他：

產(chǎn)品詳情
產(chǎn)品評(píng)價(jià)
相關(guān)產(chǎn)品
靶點(diǎn)詳情

產(chǎn)品詳情

產(chǎn)品描述：

PDPN Recombinant Monoclonal Antibody（Code: CSB-RA017739MA1HU）是針對(duì)Podoplanin（PDPN）靶點(diǎn)開(kāi)發(fā)的高特異性抗體。PDPN是一種跨膜糖蛋白，廣泛表達(dá)于淋巴管內(nèi)皮細(xì)胞、部分腫瘤細(xì)胞及間皮細(xì)胞，參與細(xì)胞遷移、血管生成和腫瘤微環(huán)境調(diào)控等生物學(xué)過(guò)程。本抗體經(jīng)ELISA、Western Blot（WB）、免疫組化（IHC）和流式細(xì)胞術(shù)（FC）嚴(yán)格驗(yàn)證，在WB實(shí)驗(yàn)中可特異性識(shí)別天然和重組PDPN蛋白，推薦使用稀釋度為1:1000-5000；IHC檢測(cè)顯示其在石蠟包埋組織中具有清晰的膜定位信號(hào)，適用稀釋度1:20-200；FC分析可有效檢測(cè)細(xì)胞表面PDPN表達(dá)，推薦稀釋度1:20-200。該抗體具備批次間一致性高、背景低的特點(diǎn)，適用于腫瘤生物學(xué)研究中腫瘤細(xì)胞侵襲轉(zhuǎn)移機(jī)制探索、淋巴管生成相關(guān)信號(hào)通路分析、組織特異性標(biāo)志物檢測(cè)等場(chǎng)景，也可用于胚胎發(fā)育或炎癥反應(yīng)中細(xì)胞-基質(zhì)相互作用研究，為體外模型構(gòu)建及分子互作分析提供可靠工具。
Uniprot No.：

Q86YL7
基因名：

PDPN
別名：

Aggrus antibody; Glycoprotein 36 KD antibody; Glycoprotein 36 antibody; gp 36 antibody; GP 38 antibody; GP 40 antibody; gp36 antibody; GP38 antibody; GP40 antibody; HT1A 1 antibody; HT1A1 antibody; hT1alpha 1 antibody; hT1alpha 2 antibody; hT1alpha1 antibody; hT1alpha2 antibody; Lung type I cell membrane associated glycoprotein antibody; Lung type I cell membrane associated glycoprotein isoform a antibody; Lung type I cell membrane associated glycoprotein T1A 2 antibody; OTS 8 antibody; OTS8 antibody; OTTHUMP00000009640 antibody; OTTHUMP00000044504 antibody; PA2.26 antibody; PA2.26 antigen antibody; Pdpn antibody; PDPN_HUMAN antibody; Podoplanin antibody; PSEC0003 antibody; PSEC0025 antibody; T1 alpha antibody; T1 ALPHA GENE antibody; T1-alpha antibody; T1A 2 antibody; T1A antibody; TI1A antibody; TIA 2 antibody; TIA2 antibody
反應(yīng)種屬：

Human, Mouse
免疫原：

Recombinant Human PDPN protein
免疫原種屬：

Homo sapiens (Human)
標(biāo)記方式：

Non-conjugated
克隆類(lèi)型：

Monoclonal
抗體亞型：

Mouse IgG
純化方式：

Affinity-chromatography
克隆號(hào)：

34B4
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
產(chǎn)品提供形式：

Liquid
應(yīng)用范圍：

ELISA, WB, IHC, FC

推薦稀釋比：

Application	Recommended Dilution
WB	1:1000-1:5000
IHC	1:20-1:200
FC	1:20-1:200

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
Immunohistochemistry (IHC) Protocol
Flow cytometry (FC) Protocol
儲(chǔ)存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評(píng)價(jià)

靶點(diǎn)詳情

功能：

Mediates effects on cell migration and adhesion through its different partners. During development plays a role in blood and lymphatic vessels separation by binding CLEC1B, triggering CLEC1B activation in platelets and leading to platelet activation and/or aggregation. Interaction with CD9, on the contrary, attenuates platelet aggregation induced by PDPN. Through MSN or EZR interaction promotes epithelial-mesenchymal transition (EMT) leading to ERZ phosphorylation and triggering RHOA activation leading to cell migration increase and invasiveness. Interaction with CD44 promotes directional cell migration in epithelial and tumor cells. In lymph nodes (LNs), controls fibroblastic reticular cells (FRCs) adhesion to the extracellular matrix (ECM) and contraction of the actomyosin by maintaining ERM proteins (EZR; MSN and RDX) and MYL9 activation through association with unknown transmembrane proteins. Engagement of CLEC1B by PDPN promotes FRCs relaxation by blocking lateral membrane interactions leading to reduction of ERM proteins (EZR; MSN and RDX) and MYL9 activation. Through binding with LGALS8 may participate in connection of the lymphatic endothelium to the surrounding extracellular matrix. In keratinocytes, induces changes in cell morphology showing an elongated shape, numerous membrane protrusions, major reorganization of the actin cytoskeleton, increased motility and decreased cell adhesion. Controls invadopodia stability and maturation leading to efficient degradation of the extracellular matrix (ECM) in tumor cells through modulation of RHOC activity in order to activate ROCK1/ROCK2 and LIMK1/LIMK2 and inactivation of CFL1. Required for normal lung cell proliferation and alveolus formation at birth. Does not function as a water channel or as a regulator of aquaporin-type water channels. Does not have any effect on folic acid or amino acid transport.
基因功能參考文獻(xiàn)：
1. Our results suggest that podoplanin expression by cancer associated fibroblasts could predict poor patient outcome in breast carcinoma PMID: 30173230
2. The mRNA high expression levels of both podoplanin and LYVE-1 genes had a statistically significantly higher rate of LN metastasis (p<0.01) and histological grade (p<0.01 for podoplanin, p<0.05 for LYVE-1). PMID: 30396932
3. It participates in tumorigenesis of odontogenic t umors. PMID: 29577431
4. expression as a predictive marker of dysplasia in oral leukoplakia PMID: 29588189
5. Lymphatic vessels were identified by the expression of podoplanin PMID: 29678517
6. Study provided evidence that high clonal expansion capacity of podoplanin-positive tumor initiating cells populations was the result of reduced cell death by podoplanin-mediated signaling. PMID: 28059107
7. TGF-beta release from platelets is necessary for podoplanin-mediated tumor invasion and metastasis in lung cancer. PMID: 28176852
8. this study suggests that podoplanin can be used as a prognostic marker to determine the malignant potential in oral leukoplakias PMID: 27153448
9. High PDPN expression is associated with Inflammatory Rheumatoid Synovial Tissues. PMID: 29377768
10. Podoplanin expression in cancer-associated fibroblasts could be an independent predictor of increased risk of recurrence in patients with p-stage IA lung adenocarcinoma. PMID: 28881047
11. Studies found that PDPN is expressed by many types of tumor cells and cancer associated fibroblasts. Moreover, high levels of PDPN expression is associated with reduced survival and cancer aggression. [review] PMID: 29575529
12. Gastric tumor cells revealed no expression of PDPN. However, PDPN was expressed in some cases in spindle-shaped stromal cells within the tumor microenvironment, except for lymphatic vessels. PDPN expression was detected in neither tumor cells nor stromal cells of metastatic regions, such as lymph node and peritoneal metastases. PMID: 29715091
13. PDPN contributes to the malignant potential of hepatocellular carcinoma. PMID: 28871005
14. In lung adenocarcinoma, the presence of podoplanin-positive cancer-associated fibroblasts (CAFs) was associated with higher numbers of single nucleotide variants (SNVs) in cancer cells. PMID: 29511884
15. The prevalence of Oct-3/4 and D2-40-(podoplanin) positive staining of germ cells in testicular biopsies of boys with cryptorchidism were in age groups less than 6 months, 100% and 50%; 6-12 months, 60% and 17%; and 1-2 years, 12% and 4%. In all cases, the Oct-3/4 and D2-40 positive germ cells turned negative and the histological pattern normalized completely with age. PMID: 27606906
16. The presence of podoplanin expression in peritumoral keratinocytes correlates with aggressive behavior in extramammary Paget's disease (EMPD). PMID: 28381343
17. PDPN was induced by hypoxia and its overexpression undergoes a reduction of adhesion, making it an anti-adhesion molecule in the absence of CCL21, in the tumor. PMID: 28416768
18. PDPN acts as an oncogene to promote hypopharyngeal cancer cell viability, migration and invasion. miR-203 directly targets PDPN to suppress its expression, thus exerting inhibitory effects on cancer metastasis. PMID: 27775879
19. podoplanin expression in cancer-related fibrotic tissues is associated with a poor prognosis, especially in patients with large tumors or lymph node metastases. PMID: 28702871
20. Data show that podoplanin (PDPN), CD106 (VCAM-1) and CD248 protein were increased in diseased compared to healthy tendon cells. PMID: 28122639
21. Increased expression of twist/podoplanin in ductal breast carcinoma was associated with shorter patient survival. PMID: 28982860
22. Study showed that podoplanin increases the motility of fibroblasts and facilitates their interaction with endothelial cells. This, respectively, favors movement of fibroblasts into the breast tumor stroma and affects tumor angiogenesis, what creates a favorable microenvironment for breast cancer progression. PMID: 28938000
23. Data suggest that podoplanin (PDPN) might be a pathogenetic determinant of malignant pleural mesothelioma (MPM) dissemination and aggressive growth and may thus be an ideal therapeutic target. PMID: 28182302
24. high podoplanin expression in primary brain tumors induces platelet aggregation, correlates with hypercoagulability, and is associated with increased risk of VTE PMID: 28073783
25. This article provides evidence supporting the implication of podoplanin expression as a marker of bad prognosis of cutaneous squamous cell carcinoma PMID: 27859466
26. A possible crosstalk between epithelial and stromal tumor cells in hepatocellular carcinoma tumor microenvironment may be mediated by podoplanin PMID: 28348421
27. interest, LpMab-17 did not bind to monkey PDPN, whereas the homology is 94% between human PDPN and monkey PDPN, indicating that the epitope of LpMab-17 is unique compared with the other anti-PDPN mAbs. The combination of different epitope-possessing mAbs could be advantageous for the PDPN-targeting diagnosis or therapy PMID: 26937552
28. podoplanin expression is significantly associated with malignant transformation of chronic lip discoid lupus erythematosus into lip squamous cell carcinoma PMID: 27240861
29. the epitope of PMab-21 was identified as Leu44-Glu48, which is corresponding to platelet aggregation-stimulating (PLAG) domain, indicating that Ser61-Ala68 of rabbit PDPN is a more appropriate epitope for immunohistochemistry compared with PLAG domain. PMab-32 could be useful for uncovering the function of rabbit PDPN PMID: 26977704
30. NZ-1 inhibits the hPDPN-CLEC-2 interaction and is also useful for anti-PA tag MAb.The minimum epitope of LpMab-13 was identified as Ala42-Asp49 of hPDPN using Western blot and flow cytometry. The combination of different epitope-possessing MAbs could be advantageous for the hPDPN-targeting diagnosis and therapy PMID: 27328060
31. Low PDPN expression is associated with Uterine Cervical Squamous Intraepithelial Lesions. PMID: 27313335
32. high tumoral podoplanin expression could independently predict an adverse clinical outcome for ccRCC patients, and it might be useful in future for clinical decision-making and therapeutic developments. PMID: 27389969
33. the present results also suggest that podoplanin+ cells can function as stromal cells for blast cell retention in the AML tumor microenvironment. PMID: 27035421
34. We revealed that podoplanin expression in Cancer-associated Fibroblasts was an independent indicator of worse prognosis, irrespective of the expression status of the tumor cells in patients with squamous cell carcinoma of the lung. PMID: 28011493
35. High podoplanin expression is associated with lymphatic spread of the breast cancer. PMID: 26881521
36. High podoplanin expression is associated with lung metastasis. PMID: 26684030
37. In esophageal squamous cell carcinoma, high p-mTOR expression was significantly associated with high podoplanin expression and high tumor grade PMID: 26722465
38. These data support a role of podoplanin as an antiapoptotic prosurvival factor in angiotensin II-induced injury of human podocytes. PMID: 26867059
39. podoplanin membrane expression, not only its localization, is a useful prognostic indicator of lung squamous cell carcinoma PMID: 26700593
40. this study uncovers a unique molecular mechanism of lymphangiogenesis in which galectin-8-dependent crosstalk among VEGF-C, podoplanin and integrin pathways plays a key role. PMID: 27066737
41. Expression of Podoplanin in Non-melanoma Skin Cancers and Actinic Keratosis PMID: 27069135
42. Almost all anti-PDPN MAbs recognize a platelet aggregation-inducing (PLAG) domain. PMID: 26492618
43. LpMab-12 could serve as a new diagnostic tool for determining whether hPDPN possesses the sialylation on Thr52, a site-specific post-translational modification critical for the hPDPN association with CLEC-2. PMID: 27031228
44. podoplanin may be considered as a predictor marker in assessing malignant transformation of premalignancies and prognosis of oral malignancy PMID: 25098985
45. Data show that the CHO cell line with the stable and high expression of recombinant podoplanin (PDPN)-enhanced green fluorescent protein (EGFP) was constructed successfully, and it could induce platelet aggregation. PMID: 26728373
46. PDPN-positive/EpCAM-positive CTC ratio is a prognostic factor and defining the ratio in patients with HNSCC might be valuable to clinical management PMID: 24844673
47. Podoplanin increased migration of tumor cells and enhanced tube formation activity in endothelial cells independent from VEGF. PMID: 26339454
48. Podoplanin overexpression is associated with osteosarcoma. PMID: 26090592
49. high podoplanin expression is associated with aggressive tumor behavior, poor prognosis and metastatic regulation through interaction with VEGF-C. PMID: 26081937
50. Podoplanin mediates extracellular matrix degradation by squamous carcinoma cells through control of invadopodia stability. PMID: 25486435
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亞細(xì)胞定位：

[Podoplanin]: Membrane; Single-pass type I membrane protein. Cell projection, lamellipodium membrane; Single-pass type I membrane protein. Cell projection, filopodium membrane; Single-pass type I membrane protein. Cell projection, microvillus membrane; Single-pass type I membrane protein. Cell projection, ruffle membrane; Single-pass type I membrane protein. Membrane raft. Apical cell membrane. Basolateral cell membrane. Cell projection, invadopodium.; [29kDa cytosolic podoplanin intracellular domain]: Cytoplasm, cytosol.
蛋白家族：

Podoplanin family
組織特異性：

Highly expressed in placenta, lung, skeletal muscle and brain. Weakly expressed in brain, kidney and liver. In placenta, expressed on the apical plasma membrane of endothelium. In lung, expressed in alveolar epithelium. Up-regulated in colorectal tumors a
數(shù)據(jù)庫(kù)鏈接：

HGNC: 29602

OMIM: 608863

KEGG: hsa:10630

STRING: 9606.ENSP00000294489

UniGene: Hs.468675

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