Recombinant Human LIMPII/SR-B2 Protein Summary
Description |
LIMPII/SR-B2 (Human) GST-Tagged Recombinant Protein
Source: Wheat Germ (in vitro) Amino Acid Sequence: MGRCCFYTAGTLSLLLLVTSVTLLVARVFQKAVDQSIEKKIVLRNGTEAFDSWEKPPLPVYTQFYFFNVTNPEEILRGETPRVEEVGPYTYRELRNKANIQFGDNGTTISAVSNKAYVFERDQSVGDPKIDLIRTLNIPVLTVIEWSQVHFLREIIEAMLKAYQQKLFVTHTVDELLWGYKDEILSLIHVFRPDISPYFGLFYEKNGTNDGDYVFLTGEDSYLNFTKIVEWNGKTSLDWWITDKCNMINGTDGDSFHPLITKDEVLYVFPSDFCRSVYITFSDYESVQGLPAFRYKVPAEILANTSDNAGFCIPEGNCLGSGVLNVSICKNGAPIIMSFPHFYQADERFVSAIEGMHPNQEDHETFVDINPLTGIILKAAKRFQINIYVKKLDDFVETGDIRTMVFPVMYLNESVHIDKETASRLKSMINTTLIITNIPYIIMALGVFFGLVFTWLACKGQGSMDEGTADERAPLIRT |
Protein/Peptide Type |
Recombinant Protein
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Gene |
SCARB2
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Applications/Dilutions
Application Notes |
Useful in Western Blot and ELISA. This protein has not been tested for any functionality. This product may contain endotoxins and is not suitable for use with live cells.
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Packaging, Storage & Formulations
Storage |
Store at -80C. Avoid freeze-thaw cycles.
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Buffer |
50 mM Tris-HCl, 10 mM reduced Glutathione, pH 8.0 in the elution buffer.
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Notes
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for Recombinant Human LIMPII/SR-B2 Protein
- AMRF
- CD36 antigen (collagen type I receptor, thrombospondin receptor)-like 2(lysosomal integral membrane protein II)
- CD36 antigen
- CD36L2
- CD36L2LIMP II
- HLGP85
- LGP85
- LIMP-2,85 kDa lysosomal sialoglycoprotein scavenger receptor class B, member 2
- LIMPII
- LIMPIICD36 antigen-like 2
- LPG85
- lysosome membrane protein 2
- Lysosome membrane protein II
- SCARB2
- Scavenger receptor class B member 2,85 kDa lysosomal membrane sialoglycoprotein
- scavenger receptor class B, member 2
- SRB2
- SR-B2
- SR-BII
Background
The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Studies of the similar protein in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. Deficiency of the similar protein in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. [provided by RefSeq]