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Thermo Fisher Scientific DMP1 Monoclonal Antibody (1D4)
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Thermo Fisher Scientific DMP1 Monoclonal Antibody (1D4)

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DMP1 단백질을 인식하는 Mouse IgG2b 단일클론 항체로, Western blot, ICC/IF, ELISA 등 다양한 응용에 적합합니다. 골 및 치아 조직 내 DMP1 발현 연구에 활용되며, 고순도 친화 크로마토그래피 정제 제품입니다.

카탈로그번호
H00001758-M01
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 08:49
Thermo Fisher Scientific H00001758-M01 DMP1 Monoclonal Antibody (1D4) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific DMP1 Monoclonal Antibody (1D4)

Applications

Application Tested Dilution
Western Blot (WB) 1–5 µg/mL
Immunocytochemistry (ICC/IF) 10 µg/mL
ELISA 1 ng/mL

Product Specifications

Specification Detail
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone 1D4
Immunogen DMP1 (NP_004398.1, 221–330 a.a.) partial recombinant protein with GST tag. MW of GST tag alone is 26 kDa.
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows:
ESIRSERGNS RMNSAGMKSK ESGENSEQAN TQDSGGSQLL EHPSRKIFRK SRISEEDDRS ELDDNNTMEE VKSDSTENSN SRDTGLSQPR RDSKGDSQED SKENLSQEES


Target Information

Dentin matrix acidic phosphoprotein (DMP1) is an extracellular matrix protein and a member of the small integrin binding ligand N-linked glycoprotein family. It plays a crucial role in bone and dentin mineralization and is found in various cells of bone and tooth tissues.
This protein has numerous acidic domains, multiple phosphorylation sites, an Arg-Gly-Asp cell attachment sequence, and a DNA binding domain. In undifferentiated osteoblasts, DMP1 acts as a nuclear protein regulating osteoblast-specific gene expression. Upon maturation, it becomes phosphorylated and exported to the extracellular matrix, where it directs mineralized matrix formation.
Mutations in the DMP1 gene cause autosomal recessive hypophosphatemia, resulting in rickets and osteomalacia. The gene structure is conserved among mammals, with two transcript variants encoding different isoforms.


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

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