CLIP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
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- Target See all CLIP2 Proteins
- CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 1
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This CLIP2 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human CLIP2 (transcript variant 1) 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 CLIP2 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
- CLIP2 (CAP-GLY Domain Containing Linker Protein 2 (CLIP2))
- Alternative Name
- Clip2 (CLIP2 Products)
- Synonyms
- CLIP Protein, CLIP-115 Protein, CYLN2 Protein, WBSCR3 Protein, WBSCR4 Protein, WSCR3 Protein, WSCR4 Protein, Cyln2 Protein, B230327O20 Protein, Clip1 Protein, mKIAA0291 Protein, wbscr4 Protein, CAP-Gly domain containing linker protein 2 Protein, CAP-GLY domain containing linker protein 2 Protein, CLIP2 Protein, Clip2 Protein, clip2 Protein
- Background
- The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
- Molecular Weight
- 115.6 kDa
- NCBI Accession
- NP_003379
- Pathways
- Microtubule Dynamics
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