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MerTK/Tyro3 Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-72735

  • Amount:

    100ul

  • Molecular Weight:

    110249/96905Da

  • Applications:

    WB;IHC-p

  • Reactivity:

    Human;Mouse;Rat

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    Synthesized peptide derived from MerTK/Tyro3 . at AA range: 690-770

  • Source:

    Polyclonal, Rabbit,IgG

  • Western Blot analysis of various cells using MerTK/Tyro3 Polyclonal Antibody

  • Gene Name:

    MERTK/TYRO3

  • Dilution:

    WB 1:500-2000;IHC-p 1:50-300

  • Protein Name:

    Tyrosine-protein kinase Mer/Tyrosine-protein kinase receptor TYRO3

  • Human Gene Id:

    10461/7301

  • Human Swiss Prot No:

    Q12866/Q06418

  • Mouse Gene Id:

    17289/22174

  • Rat Gene Id:

    65037/25232

  • Rat Swiss Prot No:

    P57097/P55146

  • Specificity:

    MerTK/Tyro3 Polyclonal Antibody detects endogenous levels of MerTK/Tyro3 protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    MERTK; MER; Tyrosine-protein kinase Mer; Proto-oncogene c-Mer; Receptor tyrosine kinase MerTK; TYRO3; BYK; DTK; RSE; SKY; Tyrosine-protein kinase receptor TYRO3; Tyrosine-protein kinase DTK; Tyrosine-protein kinase RSE; Tyrosine-protein kin

  • Observed Band(KD):

    110

  • Background:

    This gene is a member of the MER/AXL/TYRO3 receptor kinase family and encodes a transmembrane protein with two fibronectin type-III domains, two Ig-like C2-type (immunoglobulin-like) domains, and one tyrosine kinase domain. Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP). [provided by RefSeq, Jul 2008],

  • Function:

    catalytic activity:ATP + a [protein]-L-tyrosine = ADP + a [protein]-L-tyrosine phosphate.,disease:Defects in MERTK are a cause of retinitis pigmentosa (RP) [MIM:268000]. RP that leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.,function:In case of filovirus infection, seems to function as a cell entry factor.,online information:Retina International's Scientific Newsletter,similarity:Belongs to the protein kinase superfamily. Tyr protein kinase family.,similarity:Belongs to the protein kinase superfamily. Tyr protein kinase family. AXL/UFO subfamily.,similarity:Contains 1 protein kinase domain.,similarity:Contains 2 fibronectin type-III domains.,similarity:Contains 2 Ig-like C2-type (imm

  • Subcellular Location:

    Cell membrane ; Single-pass type I membrane protein .

  • Expression:

    Not expressed in normal B- and T-lymphocytes but is expressed in numerous neoplastic B- and T-cell lines. Highly expressed in testis, ovary, prostate, lung, and kidney, with lower expression in spleen, small intestine, colon, and liver.

  • Western Blot analysis of HuvEc cells using MerTK/Tyro3 Polyclonal Antibody

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Catalog Number

  • Amount:100ul
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