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中文名称：I型胶原前体蛋白1抗体
英文名称：Pro-Alpha 1 type I collagen
别\xa0\xa0\xa0\xa0名：Pro-COL1A1; Alpha 1 type I collagen; Alpha 2 type I collagen; COL1A1; COL1A2. Collagen type I; Alpha 1 type I collagen; Alpha 2 type I collagen; COL1A1; COL1A2; Collagen I alpha 1 polypeptide; Collagen I alpha 2 polypeptide; Collagen Of Skin Tendon And Bone; Collagen Type 1; Collagen type I alpha 1; Collagen type I alpha 2; OI4; Osteogenesis Imperfecta Type IV; Pro alpha 1(I) collagen; Type I procollagen; CO1A1_HUMAN; Collagen alpha-1(II) chain; Alpha-1 type II collagen; Collagen alpha-1(II) chain; Chondrocalcin; collagen alpha-1(I) chain preproprotein; PICP.\xa0\xa0
分\xa0子\xa0量：161kDa
细胞定位：分泌型蛋白\xa0
纯化方法：affinity purified by Protein A
储\xa0存\xa0液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
产品介绍：该基因编码 I 型胶原蛋白的 pro-alpha1 链，其三螺旋包括两条 alpha1 链和一条 alpha2 链。 I 型是一种形成原纤维的胶原蛋白，存在于大多数结缔组织中，并且在骨骼、角膜、真皮和肌腱中含量丰富。 该基因的突变与 I-IV 型成骨不全症、VIIA 型 Ehlers-Danlos 综合征、经典型 Ehlers-Danlos 综合征、Caffey 病和特发性骨质疏松症有关。 17 号和 22 号染色体之间的相互易位（该基因和血小板衍生生长因子 β 的基因所在的位置）与一种称为突起性皮肤纤维肉瘤的特定类型的皮肤肿瘤有关，这是由生长因子的不受调节的表达引起的。 已经为该基因鉴定了由使用交替多聚腺苷酸化信号产生的两个转录物。 [由 R. Dalgleish 提供，2008 年 2 月]
中文名称：I型胶原前体蛋白1抗体
英文名称：Pro-Alpha 1 type I collagen
别\xa0\xa0\xa0\xa0名：Pro-COL1A1; Alpha 1 type I collagen; Alpha 2 type I collagen; COL1A1; COL1A2. Collagen type I; Alpha 1 type I collagen; Alpha 2 type I collagen; COL1A1; COL1A2; Collagen I alpha 1 polypeptide; Collagen I alpha 2 polypeptide; Collagen Of Skin Tendon And Bone; Collagen Type 1; Collagen type I alpha 1; Collagen type I alpha 2; OI4; Osteogenesis Imperfecta Type IV; Pro alpha 1(I) collagen; Type I procollagen; CO1A1_HUMAN; Collagen alpha-1(II) chain; Alpha-1 type II collagen; Collagen alpha-1(II) chain; Chondrocalcin; collagen alpha-1(I) chain preproprotein; PICP.\xa0\xa0
分\xa0子\xa0量：161kDa
细胞定位：分泌型蛋白\xa0
纯化方法：affinity purified by Protein A
储\xa0存\xa0液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
产品介绍：该基因编码 I 型胶原蛋白的 pro-alpha1 链，其三螺旋包括两条 alpha1 链和一条 alpha2 链。 I 型是一种形成原纤维的胶原蛋白，存在于大多数结缔组织中，并且在骨骼、角膜、真皮和肌腱中含量丰富。 该基因的突变与 I-IV 型成骨不全症、VIIA 型 Ehlers-Danlos 综合征、经典型 Ehlers-Danlos 综合征、Caffey 病和特发性骨质疏松症有关。 17 号和 22 号染色体之间的相互易位（该基因和血小板衍生生长因子 β 的基因所在的位置）与一种称为突起性皮肤纤维肉瘤的特定类型的皮肤肿瘤有关，这是由生长因子的不受调节的表达引起的。 已经为该基因鉴定了由使用交替多聚腺苷酸化信号产生的两个转录物。 [由 R. Dalgleish 提供，2008 年 2 月]中文名称：I型胶原前体蛋白1抗体
英文名称：Pro-Alpha 1 type I collagen
别\xa0\xa0\xa0\xa0名：Pro-COL1A1; Alpha 1 type I collagen; Alpha 2 type I collagen; COL1A1; COL1A2. Collagen type I; Alpha 1 type I collagen; Alpha 2 type I collagen; COL1A1; COL1A2; Collagen I alpha 1 polypeptide; Collagen I alpha 2 polypeptide; Collagen Of Skin Tendon And Bone; Collagen Type 1; Collagen type I alpha 1; Collagen type I alpha 2; OI4; Osteogenesis Imperfecta Type IV; Pro alpha 1(I) collagen; Type I procollagen; CO1A1_HUMAN; Collagen alpha-1(II) chain; Alpha-1 type II collagen; Collagen alpha-1(II) chain; Chondrocalcin; collagen alpha-1(I) chain preproprotein; PICP.\xa0\xa0
分\xa0子\xa0量：161kDa
细胞定位：分泌型蛋白\xa0
纯化方法：affinity purified by Protein A
储\xa0存\xa0液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
产品介绍：该基因编码 I 型胶原蛋白的 pro-alpha1 链，其三螺旋包括两条 alpha1 链和一条 alpha2 链。 I 型是一种形成原纤维的胶原蛋白，存在于大多数结缔组织中，并且在骨骼、角膜、真皮和肌腱中含量丰富。 该基因的突变与 I-IV 型成骨不全症、VIIA 型 Ehlers-Danlos 综合征、经典型 Ehlers-Danlos 综合征、Caffey 病和特发性骨质疏松症有关。 17 号和 22 号染色体之间的相互易位（该基因和血小板衍生生长因子 β 的基因所在的位置）与一种称为突起性皮肤纤维肉瘤的特定类型的皮肤肿瘤有关，这是由生长因子的不受调节的表达引起的。 已经为该基因鉴定了由使用交替多聚腺苷酸化信号产生的两个转录物。 [由 R. Dalgleish 提供，2008 年 2 月]中文名称：I型胶原前体蛋白1抗体
英文名称：Pro-Alpha 1 type I collagen
别\xa0\xa0\xa0\xa0名：Pro-COL1A1; Alpha 1 type I collagen; Alpha 2 type I collagen; COL1A1; COL1A2. Collagen type I; Alpha 1 type I collagen; Alpha 2 type I collagen; COL1A1; COL1A2; Collagen I alpha 1 polypeptide; Collagen I alpha 2 polypeptide; Collagen Of Skin Tendon And Bone; Collagen Type 1; Collagen type I alpha 1; Collagen type I alpha 2; OI4; Osteogenesis Imperfecta Type IV; Pro alpha 1(I) collagen; Type I procollagen; CO1A1_HUMAN; Collagen alpha-1(II) chain; Alpha-1 type II collagen; Collagen alpha-1(II) chain; Chondrocalcin; collagen alpha-1(I) chain preproprotein; PICP.\xa0\xa0
分\xa0子\xa0量：161kDa
细胞定位：分泌型蛋白\xa0
纯化方法：affinity purified by Protein A
储\xa0存\xa0液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
产品介绍：该基因编码 I 型胶原蛋白的 pro-alpha1 链，其三螺旋包括两条 alpha1 链和一条 alpha2 链。 I 型是一种形成原纤维的胶原蛋白，存在于大多数结缔组织中，并且在骨骼、角膜、真皮和肌腱中含量丰富。 该基因的突变与 I-IV 型成骨不全症、VIIA 型 Ehlers-Danlos 综合征、经典型 Ehlers-Danlos 综合征、Caffey 病和特发性骨质疏松症有关。 17 号和 22 号染色体之间的相互易位（该基因和血小板衍生生长因子 β 的基因所在的位置）与一种称为突起性皮肤纤维肉瘤的特定类型的皮肤肿瘤有关，这是由生长因子的不受调节的表达引起的。 已经为该基因鉴定了由使用交替多聚腺苷酸化信号产生的两个转录物。 [由 R. Dalgleish 提供，2008 年 2 月]
Function:
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted "Glycine X Y" triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Procollagen type 1 is mainly synthesized by osteoblasts and, after cleavage of the N- and C-terminal extension peptides, is utilized for collagen fibril deposition in the osteoid tissue.
Function:
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted "Glycine X Y" triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Procollagen type 1 is mainly synthesized by osteoblasts and, after cleavage of the N- and C-terminal extension peptides, is utilized for collagen fibril deposition in the osteoid tissue.
Function:
Collagens are highly conserved throughout evolution and are characterised by an uninterrupted "Glycine X Y" triplet repeat that is a necessary part of the triple helical structure. Type I collagen (95 kDa) is found in bone, cornea, skin and tendon. Mutations in the encoding gene are associated with osteogenesis imperfecta, Ehlers Danlos syndrome, and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for Platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Procollagen type 1 is mainly synthesized by osteoblasts and, after cleavage of the N- and C-terminal extension peptides, is utilized for collagen fibril deposition in the osteoid tissue.
注意：
所提供的本产品仅供研究使用，不得用于人类、治疗或诊断应用。
注意：
所提供的本产品仅供研究使用，不得用于人类、治疗或诊断应用。
注意：
所提供的本产品仅供研究使用，不得用于人类、治疗或诊断应用。
注意：
所提供的本产品仅供研究使用，不得用于人类、治疗或诊断应用。
