DSPP Antikörper (AA 47-76)

Produktnummer ABIN1539403

Produktdetails anti-DSPP Antikörper

Target: DSPP (Dentin Sialophosphoprotein (DSPP))

Bindungsspezifität: AA 47-76

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DSPP Antikörper ist unkonjugiert

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

Aufreinigung: 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.

Klon: RB20942

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB: 1:2000. WB: 1:2000. FC: 1:25

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

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

Haltbarkeit: 6 months

Details zu DSPP

Target: DSPP (Dentin Sialophosphoprotein (DSPP))

Andere Bezeichnung: DSPP (DSPP Produkte)

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

Hintergrund: 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].

Molekulargewicht: 131151

Gen-ID: 1834

NCBI Accession: NP_055023

UniProt: Q9NZW4