PRPH2 (NM_000322) Human Recombinant Protein

Product Name

PRPH2 (NM_000322) Human Recombinant Protein

View all Peripherin 2/PRPH2 recombinant proteins

SKU/Catalog Number

PROTP23942

Size

20 µg

Tag

C-Myc/DDK

Description

Recombinant protein of human peripherin 2 (retinal degeneration, slow) (PRPH2)

Storage & Handling

Store at -80°C. Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. (Ship on dry ice.)

Cite This Product

PRPH2 (NM_000322) Human Recombinant Protein (Boster Biological Technology, Pleasanton CA, USA, Catalog # PROTP23942)

Form

Frozen Solution in PBS Buffer

Formulation

25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

Concentration

>50 ug/mL as determined by microplate BCA method

Purity

> 80% as determined by SDS-PAGE and Coomassie blue staining

Predicted MW

39.1 kDa

Validation Images & Assay Conditions

Click image to see more details

Coomassie blue staining of purified PRPH2 protein. The protein was produced from HEK293T cells transfected with PRPH2 cDNA clone.

Gene/Protein Information For PRPH2 (Source: Uniprot.org, NCBI)

Alternative Names

AOFMD; AVMD; CACD2; CACD2peripherin 2, homolog of mouse; DS; peripherin 2 (retinal degeneration, slow); Peripherin 2; peripherin-2; PRPH2; PRPHperipherin, photoreceptor type; rd2; RDS; Retinal degeneration slow protein; retinal degeneration, slow; retinal peripherin; RP7; Tetraspanin-22; TSPAN22; tspan-22; TSPAN22retinal degeneration, slow (retinitis pigmentosa 7) PRPH2 AOFMD, AVMD, CACD2, DS, MDBS1, PRPH, RDS, RP7, TSPAN22, rd2 peripherin 2 peripherin-2|peripherin 2 (retinal degeneration, slow)|peripherin 2, homolog of mouse|peripherin, photoreceptor type|retinal degeneration slow protein|retinal peripherin|tetraspanin-22|tspan-22

For more info on PRPH2, check out the PRPH2 Infographic

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In this infographic, you will see the following information for PRPH2: database IDs, superfamily, protein function, synonyms, molecular weight, chromosomal locations, tissues of expression, subcellular locations, post-translational modifications, and related diseases, research areas & pathways. If you want to see more information included, or would like to contribute to it and be acknowledged, please contact us at [email protected].

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