MVK Rabbit Polyclonal Antibody (CAB5354)
- SKU:
- CAB5354
- Product Type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Metabolism
Frequently bought together:
Description
Product Name: | MVK Rabbit Polyclonal Antibody |
SKU: | CAB5354 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 40-300 of human MVK (NP_000422.1). |
Sequence: | RLQP HSNG KVDL SLPN IGIK RAWD VARL QSLD TSFL EQGD VTTP TSEQ VEKL KEVA GLPD DCAV TERL AVLA FLYL YLSI CRKQ RALP SLDI VVWS ELPP GAGL GSSA AYSV CLAA ALLT VCEE IPNP LKDG DCVN RWTK EDLE LINK WAFQ GERM IHGN PSGV DNAV STWG GALR YHQG KISS LKRS PALQ ILLT NTKV PRNT RALV AGVR NRLL KFPE IVAP LLTS IDAI SLEC ERVL GEMG EAPA PEQY LVLE ELID M |
Tested Applications: | WB ELISA |
Recommended Dilution: | WB,1:500 - 1:2000 |
Synonyms: | MK; LRBP; MVLK; POROK3; MVK |
Positive Sample: | Raji,BT-474 |
Conjugate: | Unconjugated |
Cellular Localization: | Cytoplasm. |
Calculated MW: | 42kDa |
Observed MW: | 42kDa |
This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash. Alternative splicing results in multiple transcript variants.
Purification Method: | Affinity purification |
Gene ID: | 4598 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. |