ARG66555

anti-MVK antibody

anti-MVK antibody for ICC/IF,IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Monkey

Overview

Product Description Rabbit Polyclonal antibody recognizes MVK
Tested Reactivity Hu, Mk
Tested Application ICC/IF, IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name MVK
Antigen Species Human
Immunogen KLH-conjugated synthetic peptide encompassing a sequence within the center region of Human MVK.
Conjugation Un-conjugated
Alternate Names Mevalonate kinase; EC 2.7.1.36; POROK3; MK; MVLK; LRBP

Application Instructions

Application Suggestion
Tested Application Dilution
ICC/IF1:100 - 1:500
IHC-P1:100 - 1:200
WB1:500 - 1:1000
Application Note IHC-P: Antigen Retrieval: Heat mediation was performed in Sodium citrate buffer (pH 6.0).
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 42 kDa

Properties

Form Liquid
Purification Affinity purified.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 0.2% BSA.
Preservative 0.02% Sodium azide
Stabilizer 0.2% BSA
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 4598 Human MVK

Swiss-port # Q03426 Human Mevalonate kinase

Gene Symbol MVK
Gene Full Name mevalonate kinase
Background 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. [provided by RefSeq, Jul 2014]
Function May be a regulatory site in cholesterol biosynthetic pathway. [UniProt]
Cellular Localization Cytoplasm. Peroxisome. [UniProt]
Calculated MW 42 kDa