FAM65B Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
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- Target See all FAM65B Proteins
- FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 2
- Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This FAM65B protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human FAM65B (transcript variant 2) 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 FAM65B Protein
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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
- FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))
- Alternative Name
- Fam65b (FAM65B Products)
- Synonyms
- C6orf32 Protein, DIFF40 Protein, DIFF48 Protein, MYONAP Protein, PL48 Protein, 1700108N18Rik Protein, 6330500D04Rik Protein, AI225904 Protein, E430013J17Rik Protein, si:dkey-218n20.1 Protein, Ab2-162 Protein, RGD1306939 Protein, RHO family interacting cell polarization regulator 2 Protein, family with sequence similarity 65, member B Protein, ripor2 Protein, RIPOR2 Protein, Ripor2 Protein, FAM65B Protein
- Background
- This gene encodes an atypical inhibitor of the small G protein RhoA. Inhibition of RhoA activity by the encoded protein mediates myoblast fusion and polarization of T cells and neutrophils. The encoded protein is a component of hair cell stereocilia that is essential for hearing. A splice site mutation in this gene results in hearing loss in human patients.
- Molecular Weight
- 65.5 kDa
- NCBI Accession
- NP_056948
- Pathways
- Transition Metal Ion Homeostasis
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