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DMP1 Polyclonal Antibody

Catalog # Availability Size / Price Inquiry
APR18331N-1 50ul / $395
APR18331N-2 100ul / $495
APR18331N-3 200ul / $595

DMP1 Polyclonal Antibody

Brand

Leading Biology

Catalog Number

APR18331N

Product Type

Polyclonal Antibodies

Field of Research

Cell Biology & Developmental Biology>Cytoskeleton

Product Overview

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality DMP1 Polyclonal Antibody.

Molecular Weight

Calculated MW: 54kDa/55kDa Observed MW: 68kDa

Species Reactivity

Rabbit

Immunogen

Recombinant fusion protein of human DMP1 (NP_004398.1).

Cross Reactivity

Human,Mouse

Isotype

IgG

GeneID

UniProt ID

Purity

Affinity purification

Storage & Stability

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

Storage Buffer

Buffer: PBS with 50% glycerol, pH7.3.

Applications

WB,IF

Dilution

WB 1:500 - 1:2000 IF 1:20 - 1:100

Product Description

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 osteoblast-specific 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 conserved in mammals. Two transcript variants encoding different isoforms have been described for this gene.

Synonyms

DMP1; ARHP; ARHR; DMP-1; dentin matrix acidic phosphoprotein 1

Images

Western blot analysis of extracts of mouse brain, using DMP1 antibody.

Immunofluorescence analysis of U2OS cells using DMP1 antibody.

Specification

Quantity

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