DSPP antibody (AA 47-76)

Catalog No. ABIN1539403

Product Details anti-DSPP Antibody

Target: DSPP (Dentin Sialophosphoprotein (DSPP))

Binding Specificity: AA 47-76

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DSPP antibody is un-conjugated

Application: Western Blotting (WB), Flow Cytometry (FACS)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This DSPP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 47-76 amino acids of human DSPP.

Clone: RB20942

Isotype: IgG

Application Details

Application Notes: WB: 1:2000. WB: 1:2000. FC: 1:25

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: DSPP Antibody (N-term) can be refrigerated at 2-8°C for up to 6 months. For long term storage, keep at -20°C.

Expiry Date: 6 months

Target Details for DSPP

Target: DSPP (Dentin Sialophosphoprotein (DSPP))

Alternative Name: DSPP (DSPP Products)

Synonyms: DFNA39 antibody, DGI1 antibody, DMP3 antibody, DPP antibody, DSP antibody, DTDP2 antibody, Dsp antibody, RDSP2 antibody, Dmp2 antibody, Dmp3 antibody, Dpp antibody, dentin sialophosphoprotein antibody, putative mediator of RNA polymerase II transcription subunit 26 antibody, DSPP antibody, Dspp antibody, LOC551799 antibody, Patl_2314 antibody

Background: This gene encodes two principal proteins of the dentin extracellular matrix of the tooth. The preproprotein is secreted by odontoblasts and cleaved into dentin sialoprotein and dentin phosphoprotein. Dentin phosphoprotein is thought to be involved in the biomineralization process of dentin. Mutations in this gene have been associated with dentinogenesis imperfecta-1, in some individuals, dentinogenesis imperfecta occurs in combination with an autosomal dominant form of deafness. Allelic differences due to repeat polymorphisms have been found for this gene. [provided by RefSeq].

Molecular Weight: 131151

Gene ID: 1834

NCBI Accession: NP_055023

UniProt: Q9NZW4