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重組人Ⅹ型膠原蛋白

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產(chǎn)品編號bs-42277P
英文名稱Recombinant human COL10A1 protein, N-His
中文名稱重組人Ⅹ型膠原蛋白
別    名Collagen type X; Col10a 1; Collagen alpha 1(X) chain; Collagen type X alpha 1 (Schmid metaphyseal chondrodysplasia); Collagen type X alpha 1; Collagen X alpha 1 polypeptide; CollagenX; fa66d11; fb10c08; OTTHUMP00000040411; Procollagen type X alpha 1; Schmid metaphyseal chondrodysplasia; wu:fa66d11; wu:fb10c08; COAA1_HUMAN; COL10A1; Collagen alpha-1(X) chain; collagen alpha-1(X) chain precursor; Schmid metaphyseal chondrodysplasia; collagen X, alpha-1 polypeptide.  
理論分子量19.8kDa
性    狀Lyophilized or Liquid
濃    度>1mg/ml
物    種Human
序    列521-680/680
純    度>90% as determined by SDS-PAGE
純化方法AC
內(nèi)毒素Not analyzed
表達(dá)系統(tǒng)E.coli
標(biāo)簽N-His
緩 沖 液20mM Tris-Hcl (pH=8.0)
保存條件Stored at -70℃ or -20℃. 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.
產(chǎn)品介紹This gene encodes the alpha chain of type X collagen, a short chain collagen expressed by hypertrophic chondrocytes during endochondral ossification. Unlike type VIII collagen, the other short chain collagen, type X collagen is a homotrimer. Mutations in this gene are associated with Schmid type metaphyseal chondrodysplasia (SMCD) and Japanese type spondylometaphyseal dysplasia (SMD). [provided by RefSeq, Jul 2008].

SWISS:
A1L4P2

Gene ID:
1300

Ⅹ型膠原是一種短鏈的非纖維性膠原,正常存在于軟骨化骨中心及骨骺軟骨生長板內(nèi),僅見于軟骨細(xì)胞肥大區(qū)及鈣化區(qū)前沿,在關(guān)節(jié)軟骨見于鈣化軟骨層,由肥大軟骨細(xì)胞特異表達(dá),只短暫出現(xiàn),可能參與軟骨鈣化的調(diào)節(jié),是正常和異常骨形成的標(biāo)志。
有學(xué)者認(rèn)為:Ⅹ型膠原在骨性關(guān)節(jié)病中可作為軟骨細(xì)胞表型不可逆轉(zhuǎn)的診斷標(biāo)志 ,是大量關(guān)節(jié)軟骨細(xì)胞發(fā)生凋亡,最終導(dǎo)致關(guān)節(jié)軟骨變薄,關(guān)節(jié)下骨變硬、增厚的主要原因。
產(chǎn)品圖片
The purity of the protein is greater than 90% as determined by reducing SDS-PAGE.
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