PRPH2 Monoclonal antibody, PBS Only (Capture)

PRPH2 Monoclonal Antibody for WB, Cytometric bead array, Indirect ELISA

Host / Isotype

Mouse / IgG2a

Reactivity

human, mouse, rat, rabbit

Applications

WB, Cytometric bead array, Indirect ELISA

Conjugate

Unconjugated

CloneNo.

2F11A1

Cat no : 68780-1-PBS

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Synonyms

Peripherin-2, Peripherin2, Peripherin 2, AVMD, AOFMD



产品信息

68780-1-PBS targets PRPH2 as part of a matched antibody pair:

MP50146-1: 68780-1-PBS capture and 68780-2-PBS detection (validated in Cytometric bead array, Sandwich ELISA)

Unconjugated mouse monoclonal antibody pair in PBS only (BSA and azide free) storage buffer at a concentration of 1 mg/mL, ready for conjugation.

This conjugation ready format makes antibodies ideal for use in many applications including: ELISAs, multiplex assays requiring matched pairs, mass cytometry, and multiplex imaging applications.Antibody use should be optimized by the end user for each application and assay.

Tested Applications WB, Cytometric bead array, Indirect ELISA Application Description
Tested Reactivity human, mouse, rat, rabbit
Immunogen PRPH2 fusion protein Ag12555 种属同源性预测
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Full Name peripherin 2 (retinal degeneration, slow)
Synonyms Peripherin-2, Peripherin2, Peripherin 2, AVMD, AOFMD
Calculated Molecular Weight 346 aa, 39 kDa
Observed Molecular Weight35-39 kDa
GenBank Accession NumberBC074720
Gene Symbol PRPH2
Gene ID (NCBI) 5961
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
UNIPROT IDP23942
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.
The product is shipped with ice packs. Upon receipt, store it immediately at -80°C

背景介绍

Peripherin-2 (PRPH2), also known as retinal degeneration slow protein (RDS), is a photoreceptor-specific tetraspanin protein implicated in outer segment disk morphogenesis. It may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Mutations in peripherin-2 are responsible for various retinal degenerative diseases including autosomal dominant retinitis pigmentosa (ADRP).