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MYOT Rabbit Polyclonal Antibody

CAT: 0013-GTR18338133Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18338133Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Anti-MYOT Antibody. Tested in WB, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat.
Product Name Alternative
57 kDa cytoskeletal protein; LGMD1; LGMD1A; MYOT; myotilin; TTID
UniProt
Q9UBF9
Reactivity
Human, Mouse, Rat
Immunogen
E.coli-derived human MYOT recombinant protein (Position: H9-E494) . Human MYOT shares 88.9% amino acid (aa) sequence identity with mouse MYOT.
Target
Myotilin
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Musculoskeletal & Connective Tissue Research
Purification
Immunogen affinity purified.
Concentration
Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Dilution
Western blot, 0.25-0.5 μg/ml, Human, Mouse, Rat Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/ml, Human Immunocytochemistry/Immunofluorescence, 5 μg/ml, Human Flow Cytometry (Fixed), 1-3 μg/1x10^6 cells, Human ELISA, 0.1-0.5 μg/ml
Form
Lyophilized
Molecular Weight
55 kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
ELISA, FC, ICC, IHC, WB
Host or Source
Rabbit
Preservative
Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
Isotype
IgG

UniProtKB · Q9UBF9

Myotilin

MYOTI_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9UBF9
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
MYOT
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A0A0C4DFM5, A0A4R6, B4DT79
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Molecular function

Actin-bindingMuscle protein

Coding sequence diversity

Alternative splicing

Cellular component

Cell membraneCytoplasmCytoskeletonMembrane

Disease

Disease variantLimb-girdle muscular dystrophyMyofibrillar myopathy

Domain

Immunoglobulin domainRepeat

PTM

Methylation

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