Recombinant Human RD3 Protein, Myc/DDK-tagged, C13 and N15-labeled

• Cat.No.: RD3-5664H
• Product Overview: RD3 MS Standard C13 and N15-labeled recombinant protein (NP_898882) with a C-terminal MYC/DDK tag, was expressed in HEK293 cells.

Specification

• Species: Human
• Source: HEK293
• Tag: DDK&Myc
• Description: This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants.
• Molecular Mass: 22.7 kDa
• AA Sequence: MSLISWLRWNEAPSRLSTRSPAEMVLETLMMELTGQMREAERQQRERSNAVRKVCTGVDYSWLASTPRSTYDLSPIERLQLEDVCVKIHPSYCGPAILRFRQLLAEQEPEVQEVSQLFRSVLQEVLERMKQEEEAHKLTRQWSLRPRGSLATFKTRARISPFASDIRTISEDVERDTPPPLRSWSMPEFRAPKADTRTRPLEQKLISEEDLAANDILDYKDDDDKV
• Purity: > 80% as determined by SDS-PAGE and Coomassie blue staining
• Stability: Stable for 3 months from receipt of products under proper storage and handling conditions.
• Storage: Store at -80 centigrade. Avoid repeated freeze-thaw cycles.
• Concentration: 50 μg/mL as determined by BCA
• Storage Buffer: 100 mM glycine, 25 mM Tris-HCl, pH 7.3.

Gene Information

• Gene Name: RD3 retinal degeneration 3 [ Homo sapiens (human) ]
• Official Symbol: RD3
• Synonyms: RD3; retinal degeneration 3; C1orf36, chromosome 1 open reading frame 36; protein RD3; LCA12; C1orf36
• Gene ID: 343035
• mRNA Refseq: NM_183059
• Protein Refseq: NP_898882
• MIM: 180040
• UniProt ID: Q7Z3Z2