LCK Rabbit Polyclonal Antibody (CAB2177)
- SKU:
- CAB2177
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Immunology
Frequently bought together:
Description
Product Name: | LCK Rabbit Polyclonal Antibody |
SKU: | CAB2177 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-240 of human LCK (NP_005347.3). |
Sequence: | MGCG CSSH PEDD WMEN IDVC ENCH YPIV PLDG KGTL LIRN GSEV RDPL VTYE GSNP PASP LQDN LVIA LHSY EPSH DGDL GFEK GEQL RILE QSGE WWKA QSLT TGQE GFIP FNFV AKAN SLEP EPWF FKNL SRKD AERQ LLAP GNTH GSFL IRES ESTA GSFS LSVR DFDQ NQGE VVKH YKIR NLDN GGFY ISPR ITFP GLHE LVRH YTNA SDGL CTRL SRPC QTQK PQKP WWED EWEV |
Tested Applications: | WB IHC-P ELISA |
Recommended Dilution: | WB,1:500 - 1:1000 IHC-P,1:50 - 1:200 |
Synonyms: | LSK; YT16; IMD22; p56lck; pp58lck; LCK |
Positive Sample: | Raji,Mouse lung,Mouse thymus |
Conjugate: | Unconjugated |
Cellular Localization: | Cell membrane, Cytoplasm, Cytoplasmic side, Lipid-anchor. |
Calculated MW: | 58kDa |
Observed MW: | 58kDa |
This gene is a member of the Src family of protein tyrosine kinases (PTKs). The encoded protein is a key signaling molecule in the selection and maturation of developing T-cells. It contains N-terminal sites for myristylation and palmitylation, a PTK domain, and SH2 and SH3 domains which are involved in mediating protein-protein interactions with phosphotyrosine-containing and proline-rich motifs, respectively. The protein localizes to the plasma membrane and pericentrosomal vesicles, and binds to cell surface receptors, including CD4 and CD8, and other signaling molecules. Multiple alternatively spliced variants encoding different isoforms have been described.
Purification Method: | Affinity purification |
Gene ID: | 3932 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.01% thimerosal,50% glycerol,pH7.3. |