SR-B2/LIMPII Rabbit Polyclonal Antibody (CAB12723)
- SKU:
- CAB12723
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Immunology
Description
Product Name: | SR-B2/LIMPII Rabbit Polyclonal Antibody |
SKU: | CAB12723 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 200-380 of human SR-B2/LIMPII (NP_005497.1). |
Sequence: | GLFY EKNG TNDG DYVF LTGE DSYL NFTK IVEW NGKT SLDW WITD KCNM INGT DGDS FHPL ITKD EVLY VFPS DFCR SVYI TFSD YESV QGLP AFRY KVPA EILA NTSD NAGF CIPE GNCL GSGV LNVS ICKN GAPI IMSF PHFY QADE RFVS AIEG MHPN QEDH ETFV DINP LTGI ILKA A |
Tested Applications: | WB IF/ICC ELISA |
Recommended Dilution: | WB,1:1000 - 1:3000 IF/ICC,1:50 - 1:200 |
Synonyms: | AMRF; EPM4; LGP85; CD36L2; HLGP85; LIMP-2; LIMPII; SR-BII; SR-B2/LIMPII |
Positive Sample: | HeLa,HepG2,Mouse heart,Mouse Lung,Mouse Liver,Rat Lung |
Conjugate: | Unconjugated |
Cellular Localization: | Lysosome membrane, Multi-pass membrane protein. |
Calculated MW: | 54kDa |
Observed MW: | 80kDa |
The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Purification Method: | Affinity purification |
Gene ID: | 950 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.01% thimerosal,50% glycerol,pH7.3. |