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Thermo Fisher Scientific DMP1 Polyclonal Antibody
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Thermo Fisher Scientific DMP1 Polyclonal Antibody

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DMP1 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot과 IHC(Paraffin)에서 검증됨. 인간, 생쥐, 비인간 영장류에 반응. Affinity chromatography로 정제된 액상 항체이며, PBS/glycerol buffer에 보관. 연구용으로만 사용 가능.

카탈로그번호
PA5103323
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 12:12
Thermo Fisher Scientific PA5103323 DMP1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific DMP1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:1,000–1:3,000 View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200 -

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Non-human primate
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human DMP1 (Accession Q13316), corresponding to amino acid residues D478–Y513
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2852668

Product Specific Information

This antibody detects endogenous levels of total DMP1.


Target Information

Dentin matrix acidic phosphoprotein (DMP1) is an extracellular matrix protein and a member of the small integrin binding ligand N-linked glycoprotein (SIBLING) family. It is essential for proper mineralization of bone and dentin and is expressed in various bone and tooth tissue cells.
The protein includes multiple acidic domains, phosphorylation sites, an RGD cell attachment sequence, and a DNA-binding domain. In undifferentiated osteoblasts, DMP1 acts as a nuclear protein regulating osteoblast-specific gene expression. During osteoblast maturation, it becomes phosphorylated and exported to the extracellular matrix, facilitating mineralized matrix formation.
Mutations in the DMP1 gene can lead to autosomal recessive hypophosphatemia, resulting in rickets and osteomalacia. The gene structure is conserved among mammals, and two transcript variants encoding different isoforms have been identified.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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