Description
Product Name: | Erlin-2 Rabbit mAb |
Product Code: | CAB0781 |
Size: | 20uL, 50uL, 100uL |
Synonyms: | ERLIN2, C8orf2, Erlin-2, NET32, SPFH2, SPG18, erlin-2 |
Applications: | WB, IHC |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | A synthesized peptide derived from human Erlin-2. |
Applications: | WB, IHC |
Recommended Dilutions: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | 293T, PC-3, OVCAR3, C2C12 |
Immunogen: | A synthesized peptide derived from human Erlin-2. |
Purification Method: | Affinity purification |
Storage: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | Email for sequence |
Gene ID: | 11160 |
Uniprot: | O94905 |
Cellular Location: | Endoplasmic reticulum membrane, Single-pass type II membrane protein |
Calculated MW: | 38kDa |
Observed MW: | 43KDa |
UniProt Protein Function: | SPFH2: Component of the ERLIN1/ERLIN2 complex which mediates the endoplasmic reticulum-associated degradation (ERAD) of inositol 1,4,5-trisphosphate receptors (IP3Rs). Also involved in ITPR1 degradation by the ERAD pathway. Interacts with activated ITPR1, independently of the degree of ITPR1 polyubiquitination. Forms a heteromeric complex with ERLIN1. Ubiquitous. Belongs to the band 7/mec-2 family. 3 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Endoplasmic reticulum; Membrane protein, integral Chromosomal Location of Human Ortholog: 8p11.2 Cellular Component: cytoplasm; endoplasmic reticulum; endoplasmic reticulum membrane; lipid raft; plasma membrane; protein complex Molecular Function:cholesterol binding; protein binding; protein-tyrosine kinase activity; ubiquitin protein ligase binding Biological Process: ER-associated protein catabolic process; negative regulation of cholesterol biosynthetic process; negative regulation of fatty acid biosynthetic process; SREBP-mediated signaling pathway Disease: Spastic Paraplegia 18, Autosomal Recessive |
NCBI Summary: | This gene encodes a member of the SPFH domain-containing family of lipid raft-associated proteins. The encoded protein is localized to lipid rafts of the endoplasmic reticulum and plays a critical role in inositol 1,4,5-trisphosphate (IP3) signaling by mediating ER-associated degradation of activated IP3 receptors. Mutations in this gene are a cause of spastic paraplegia-18 (SPG18). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012] |
UniProt Code: | O94905 |
NCBI GenInfo Identifier: | 38257366 |
NCBI Gene ID: | 11160 |
NCBI Accession: | O94905.1 |
UniProt Secondary Accession: | O94905,Q6NW21, Q86VS6, Q86W49, A0JLQ1, A8K5S9, B4DM38 D3DSW0, |
UniProt Related Accession: | O94905 |
Molecular Weight: | 22,939 Da |
NCBI Full Name: | Erlin-2 |
NCBI Synonym Full Names: | ER lipid raft associated 2 |
NCBI Official Symbol: | ERLIN2 |
NCBI Official Synonym Symbols: | NET32; SPFH2; SPG18; C8orf2; Erlin-2 |
NCBI Protein Information: | erlin-2 |
UniProt Protein Name: | Erlin-2 |
UniProt Synonym Protein Names: | Endoplasmic reticulum lipid raft-associated protein 2; Stomatin-prohibitin-flotillin-HflC/K domain-containing protein 2; SPFH domain-containing protein 2 |
Protein Family: | Erlin |
UniProt Gene Name: | ERLIN2 |
UniProt Entry Name: | ERLN2_HUMAN |