RAG2 (NM_000536) Human Recombinant Protein
CAT#: TP761796
Purified recombinant protein of Human recombination activating gene 2 (RAG2), transcript variant 1, full length, with N-terminal GST and C-terminal His tag, expressed in E. coli, 50ug
View other "RAG2" proteins (2)
Need it in bulk or customized? Get a free quote |
CNY 2,040.00
货期*
现货
规格
经常一起买 (1)
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length RAG2
|
Tag | N-GST and C-His |
Predicted MW | 87.1 kDa |
Concentration | >0.05 µg/µL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 50 mM Tris-HCl, pH 8.0, 8 M urea |
Note | For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process. |
Storage | Store at -80°C. |
Stability | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_000527 |
Locus ID | 5897 |
UniProt ID | P55895 |
Refseq Size | 2457 |
Cytogenetics | 11p12 |
Refseq ORF | 1581 |
Synonyms | RAG-2 |
Summary | This gene encodes a protein that is involved in the initiation of V(D)J recombination during B and T cell development. This protein forms a complex with the product of the adjacent recombination activating gene 1, and this complex can form double-strand breaks by cleaving DNA at conserved recombination signal sequences. The recombination activating gene 1 component is thought to contain most of the catalytic activity, while the N-terminal of the recombination activating gene 2 component is thought to form a six-bladed propeller in the active core that serves as a binding scaffold for the tight association of the complex with DNA. A C-terminal plant homeodomain finger-like motif in this protein is necessary for interactions with chromatin components, specifically with histone H3 that is trimethylated at lysine 4. Mutations in this gene cause Omenn syndrome, a form of severe combined immunodeficiency associated with autoimmune-like symptoms. [provided by RefSeq, Jul 2008] |
Protein Families | Druggable Genome |
Protein Pathways | Primary immunodeficiency |
Documents
FAQs |
SDS |
Resources
蛋白相关资源 |
Customer
Reviews
Loading...