貨號
產品規格
售價
備注
BN42178R-50ul
50ul
¥1486.00
交叉反應:Mouse,Rat(predicted:Human,Chicken,Dog,Cow,Rabbit) 推薦應用:WB,IHC-P,IHC-F,IF,ELISA
BN42178R-100ul
100ul
¥2360.00
交叉反應:Mouse,Rat(predicted:Human,Chicken,Dog,Cow,Rabbit) 推薦應用:WB,IHC-P,IHC-F,IF,ELISA
BN42178R-200ul
200ul
¥3490.00
交叉反應:Mouse,Rat(predicted:Human,Chicken,Dog,Cow,Rabbit) 推薦應用:WB,IHC-P,IHC-F,IF,ELISA
產品描述
英文名稱 | Collagen X |
中文名稱 | Ⅹ型膠原抗體 |
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. |
研究領域 | 細胞生物 免疫學 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應 | Mouse, Rat, (predicted: Human, Chicken, Dog, Cow, Rabbit, ) |
產品應用 | WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 73kDa |
細胞定位 | 細胞外基質 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human Collagen X:601-680/680 |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
儲 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存條件 | Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. |
PubMed | PubMed |
產品介紹 | 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]. Function: Type X collagen is a product of hypertrophic chondrocytes and has been localized to presumptive mineralization zones of hyaline cartilage. Subunit: Homotrimer. Subcellular Location: Secreted, extracellular space, extracellular matrix. Tissue Specificity: Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains. DISEASE: Schmid type metaphyseal chondrodysplasia (SMCD) [MIM:156500]: Dominantly inherited disorder of the osseous skeleton. The cardinal features of the phenotype are mild short stature, coxa vara and a waddling gait. Radiography usually shows sclerosis of the ribs, flaring of the metaphyses, and a wide irregular growth plate, especially of the knees. A variant form of SMCD is spondylometaphyseal dysplasia Japanese type. It is characterized by spinal involvement comprising mild platyspondyly, vertebral body abnormalities, and end-plate irregularity. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Contains 1 C1q domain. SWISS: A1L4P2 Gene ID: 1300 Database links: Entrez Gene: 1300 Human Entrez Gene: 12813 Mouse Omim: 120110 Human SwissProt: A1L4P2 Human SwissProt: Q03692 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 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,僅見于軟骨細胞肥大區及鈣化區前沿,在關節軟骨見于鈣化軟骨層,由肥大軟骨細胞特異表達,只短暫出現,可能參與軟骨鈣化的調節,是正常和異常骨形成的標志。 有學者認為:Ⅹ型膠原在骨性關節病中可作為軟骨細胞表型不可逆轉的診斷標志 ,是大量關節軟骨細胞發生凋亡,最終導致關節軟骨變薄,關節下骨變硬、增厚的主要原因。 |