WDR73 Protein (Myc-DYKDDDDK Tag)
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- Target See all WDR73 Proteins
- WDR73 (WD Repeat Domain 73 (WDR73))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This WDR73 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human WDR73 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product WDR73 Protein
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WD Repeat Domain 73 (WDR73) (AA 1-378) protein (GST tag)
WDR73 Origin: Human Host: Wheat germ Recombinant ELISA, WB, AA, AP
WD Repeat Domain 73 (WDR73) (AA 1-378) protein (Strep Tag)Crystallography grade WDR73 Origin: Human Host: Tobacco (Nicotiana tabacum) Recombinant >80 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. ELISA, WB, SDS
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- WDR73 (WD Repeat Domain 73 (WDR73))
- Alternative Name
- Wdr73 (WDR73 Products)
- Synonyms
- 1200011I23Rik Protein, 2410008B13Rik Protein, AI848574 Protein, C85352 Protein, zgc:112071 Protein, WD repeat domain 73 Protein, WD repeat domain 73 L homeolog Protein, WDR73 Protein, Wdr73 Protein, wdr73.L Protein, wdr73 Protein
- Background
- The protein encoded by this gene is thought to contain multiple WD40 repeats. WD40 repeats are motifs that contain 40-60 amino acids, and usually end with Trp-Asp (WD). This protein is found in the cytoplasm during interphase, but accumulates at the spindle poles and astral microtubules during mitosis. Reduced expression of this gene results in abnormalities in the size and morphology of the nucleus. Mutations in this gene have been associated with Galloway-Mowat syndrome PMID: 25466283), which is a rare autosomal recessive disorder that affects both the central nervous system and kidneys. Alternative splicing results in multiple transcript variants.
- Molecular Weight
- 41.5 kDa
- NCBI Accession
- NP_116245
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