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CK3 Rabbit pAb (bs-3646R)  
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產品編號 bs-3646R
英文名稱 CK3 Rabbit pAb
中文名稱 細胞角蛋白3抗體
別    名 Cytokeratin 3; 65 kDa cytokeratin; CK 3; CK-3; CK3; Cytokeratin-3; Cytokeratin3; FLJ95909; K2C3_HUMAN; K3; K3; Keratin 3; Keratin; Keratin type II cytoskeletal 3; Keratin-3; Keratin3; KRT 3; KRT3; type II cytoskeletal 3; Type-II keratin Kb3.  
Specific References  (3)     |     bs-3646R has been referenced in 3 publications.
[IF=14.593] Binbin He. et al. 3D printed biomimetic epithelium/stroma bilayer hydrogel implant for corneal regeneration. Bioact Mater. 2022 Jan;:  IF ;  Rabbit.  
[IF=3.457] Wu Y et al. Tetramethylpyrazine (TMP) ameliorates corneal neovascularization via regulating cell infiltration into cornea after alkali burn. (2019)Biomedicine & Pharmacotherapy, 109, 1041–1051.  IF ;  Mouse.  
[IF=1.291] Duan CY et al. Limbal niche cells can reduce the angiogenic potential of cultivated oral mucosal epithelial cells. Cell Mol Biol Lett. 2019 Apr 4;24:3.  ICF ;  Rat.  
研究領域 腫瘤  神經生物學  信號轉導  細胞類型標志物  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Dog,Horse)
產品應用 WB=1:500-2000,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 65 kDa
檢測分子量
細胞定位 細胞漿 細胞外基質 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CK3: 221-320/628 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the corneal epithelium with family member KRT12 and mutations in these genes have been associated with Meesmann's Corneal Dystrophy. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]

Subunit:
Heterotetramer of two type I and two type II keratins. Keratin-3 associates with keratin-12.

Tissue Specificity:
Cornea specific.

DISEASE:
Corneal dystrophy, Meesmann (MECD) [MIM:122100]: An autosomal dominant corneal disease characterized by fragility of the anterior corneal epithelium. Patients are usually asymptomatic until adulthood when rupture of the corneal microcysts may cause erosions, producing clinical symptoms such as photophobia, contact lens intolerance and intermittent diminution of visual acuity. Rarely, subepithelial scarring causes irregular corneal astigmatism and permanent visual impairment. Histological examination shows a disorganized and thickened epithelium with widespread cytoplasmic vacuolation and numerous small, round, debris-laden intraepithelial cysts. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the intermediate filament family.

SWISS:
P12035

Gene ID:
3850

Database links:

Entrez Gene: 281267 Cow

Entrez Gene: 3850 Human

Omim: 148043 Human

SwissProt: P12035 Human

SwissProt: Q29426 Rabbit

Unigene: 680652 Human



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