FKBP14 purified MaxPab mouse polyclonal antibody (B01P) View larger

FKBP14 purified MaxPab mouse polyclonal antibody (B01P)

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Data sheet of FKBP14 purified MaxPab mouse polyclonal antibody (B01P)

BrandAbnova
Product typePrimary antibodies
ReactivityHuman
Host speciesMouse
ApplicationsWB-Ti,WB-Tr

More info about FKBP14 purified MaxPab mouse polyclonal antibody (B01P)

Brand: Abnova
Reference: H00055033-B01P
Product name: FKBP14 purified MaxPab mouse polyclonal antibody (B01P)
Product description: Mouse polyclonal antibody raised against a full-length human FKBP14 protein.
Gene id: 55033
Gene name: FKBP14
Gene alias: FKBP22|FLJ20731
Gene description: FK506 binding protein 14, 22 kDa
Genbank accession: NM_017946.2
Immunogen: FKBP14 (NP_060416.1, 1 a.a. ~ 211 a.a) full-length human protein.
Immunogen sequence/protein sequence: MRLFLWNAVLTLFVTSLIGALIPEPEVKIEVLQKPFICHRKTKGGDLMLVHYEGYLEKDGSLFHSTHKHNNGQPIWFTLGILEALKGWDQGLKGMCVGEKRKLIIPPALGYGKEGKGKIPPESTLIFNIDLLEIRNGPRSHESFQEMDLNDDWKLSKDEVKAYLKKEFEKHGAVVNESHHDALVEDIFDKEDEDKDGFISAREFTYKHDEL
Protein accession: NP_060416.1
Storage buffer: In 1x PBS, pH 7.4
Storage instruction: Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
Quality control testing: Antibody reactive against mammalian transfected lysate.
Product type: Primary antibodies
Host species: Mouse
Antigen species / target species: Human
Reactivity: Human
Application image: H00055033-B01P-13-15-1.jpg
Application image note: Western Blot analysis of FKBP14 expression in transfected 293T cell line (H00055033-T01) by FKBP14 MaxPab polyclonal antibody.

Lane 1: FKBP14 transfected lysate(23.21 KDa).
Lane 2: Non-transfected lysate.
Applications: WB-Ti,WB-Tr
Shipping condition: Dry Ice
Publications: Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss.Baumann M, Giunta C, Krabichler B, Ruschendorf F, Zoppi N, Colombi M, Bittner RE, Quijano-Roy S, Muntoni F, Cirak S, Schreiber G, Zou Y, Hu Y, Romero NB, Carlier RY, Amberger A, Deutschmann A, Straub V, Rohrbach M, Steinmann B, Rostasy K, Karall D, Bonnemann CG, Zschocke J, Fauth C.
Am J Hum Genet. 2012 Feb 10;90(2):201-16. Epub 2012 Jan 19.

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