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Anti-Human MYOT Polyclonal Antibody

Catalog #:   PHK55901 Specific References (10) DATASHEET
Host species: Rabbit
Isotype: IgG
Applications: ELISA, IHC, WB
Accession: Q9UBF9
Overview

Catalog No.

PHK55901

Species reactivity

Human

Host species

Rabbit

Isotype

IgG

Clonality

Polyclonal

Immunogen

E. coli - derived recombinant Human MYOT (Arg251-Thr441).

Tested applications

ELISA: 1:4000-1:8000, IHC: 1:50-1:100, WB: 1:1000-1:4000

Target

MYOT, 57 kDa cytoskeletal protein, TTID, Titin immunoglobulin domain protein, Myotilin, Myofibrillar titin-like Ig domains protein

Purification

Purified by antigen affinity column.

Accession

Q9UBF9

Applications

ELISA, IHC, WB

Form

Liquid

Storage buffer

0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Data Image
  • Western Blot
    Recombinant Protein lysates were subjected to SDS PAGE followed by western blot with MYOT antibody (PHK55901) at 1 μg/ml.

    Lane 1: Recombinant protein

    Second Ab: Goat Anti-Rabbit IgG H&L Polyclonal antibody, HRP (PTB96431) at 0.1 μg/mL.

    Predict MW: 24 kDa
    Observed MW: 24 kDa
References

Solution structure of the first immunoglobulin domain of human myotilin., PMID:19418025

TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies., PMID:19225410

Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study., PMID:19151983

In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy., PMID:19050726

Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene., PMID:18653338

Expression of mutant ubiquitin (UBB+1) and p62 in myotilinopathies and desminopathies., PMID:17931355

Beyond LGMD1A: myotilin is a component of central core lesions and nemaline rods., PMID:12899871

Myotilin, the limb-girdle muscular dystrophy 1A (LGMD1A) protein, cross-links actin filaments and controls sarcomere assembly., PMID:12499399

Indications for a novel muscular dystrophy pathway. gamma-filamin, the muscle-specific filamin isoform, interacts with myotilin., PMID:11038172

Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy., PMID:10369880

Datasheet
$ 170
Product specifications
50 μg 170 100 μg 280

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Distributor list

For research use only. Not for human or drug use.

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Anti-Human MYOT Polyclonal Antibody [PHK55901]
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