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产地 | 中国 |
品牌 | Chemstan |
保存条件 | Use a manual defrost freezer and avoid repeated freeze thaw cycles.Store at 4 °C for frequent use.Store at -20 to -80 °C for twelve months from the date of receipt. |
货号 | ATA28192 |
用途 | 仅供科研用 |
应用范围 | WB,ELISA |
CAS编号 | |
抗体名 | DMP1 rabbit Polyclonal Antibody |
克隆性 | |
靶点 | DMP1 |
适应物种 | Human |
形态 | Liquid |
宿主 | Rabbit |
包装规格 | 100ul |
亚型 | |
纯度 | % |
标识物 | Unconjugated |
浓度 | 1mg/ml% |
免疫原 | Synthesized peptide derived from human protein . at AA range: 430-510 |
是否进口 | 否 |
用一种包含多种抗原决定簇的抗原免疫动物,可刺激机体多个B细胞*产生针对多种抗原表位的不同抗体。所获得的免疫血清实际上是含有多种抗体的混合物。
产品概述
产品名(Product Name)
DMP1 rabbit Polyclonal Antibody
货号(Catalog No.)
ATA28192
种类(Category)
Primary antibodies
表达宿主(Host)
Rabbit
反应种属(Species specificity)
Human
应用实验(Tested applications)
WB,ELISA
*性(Clonality)
Polyclonal
偶连物(Conjugation)
Unconjugated
免疫原(Immunogen)
Synthesized peptide derived from human protein . at AA range: 430-510
产品性能
状态(Form)
Liquid
存放条件(Storage)
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 4 °C for frequent use. Store
at -20 to -80 °C for twelve months from the date of receipt.
纯化方式(Purity)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific
immunogen.
应用
WB 1:500-2000 ELISA 1:5000-20000
产品背景
dentin matrix acidic phosphoprotein 1(DMP1) Homo sapiens Dentin matrix acidic phosphoprotein is an extracellular matrix protein and a member of the small integrin binding ligand N-linked glycoprotein family. This protein, which is critical for proper mineralization of bone and dentin, is present in diverse cells of bone and tooth tissues. The protein contains a large number of acidic domains, multiple phosphorylation sites, a functional arg-gly-asp cell attachment sequence, and a DNA binding domain. In undifferentiated osteoblasts it is primarily a nuclear protein that regulates the expression of osteoblastspecific genes. During osteoblast maturation the protein becomes phosphorylated and is exported to the extracellular matrix, where it orchestrates mineralized matrix formation. Mutations in the gene are known to cause autosomal recessive hypophosphatemia, a disease that manifests as rickets and osteomalacia. The gene structure is conser