![MVK antibody [N3C3]](https://www.genetex.com/upload/website/prouct_img/normal/GTX107761/GTX107761_IHC_w_23060120_242.webp)
![MVK antibody [N3C3]](https://www.genetex.com/upload/website/prouct_img/normal/GTX107761/GTX107761_WB_w_23060120_905.webp)
GTX107761
MVK antibody [N3C3]
Cannot supply to this region.
- SKU:
- GTX107761
- Additional Names:
- mevalonate kinase , LRBP , MK , MVLK , POROK3
- Application:
- WB, IHC-P
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- 0.1M Tris, 0.1M Glycine, 10% Glycerol, 0.01% Thimerosal.
- Immunogen:
- Recombinant protein encompassing a sequence within the center region of human MVK. The exact sequence is proprietary.
- Clone:
- N3C3
- Uniprot:
- Q03426
- Synonyms:
- LH receptor mRNA-binding protein;LRBP;mevalonate kinase;mevalonate kinase 1;MK;MVLK;POROK3
- Extra Details:
- 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. Two transcript variants that encode the same protein have been found for this gene. [provided by RefSeq]
- Shipping Conditions:
- Blue Ice