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MYLPF Polyclonal Antibody
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FIGURE: 1 / 1
MYLPF Antibody (PA5-36041) in WB
Western blot analysis of MYLPF in Lane 1: the Muscle tissue lysate of mouse (40 µg), Lane 2: the Muscle tissue lysate of rat (40 µg), Lane 3: LOVO whole cell lysate (40 µg), Lane 4: H1792 whole cell lysate (40 µg). Samples were incubated with MYLPF polyclonal antibody (Product # PA5-36041) at a dilution of 1:500.
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Product Details
PA5-36041
Product Specifications
Species Reactivity
Human,
Mouse,
Rat
Host/Isotype
Rabbit
/ IgG
Class
Polyclonal
Type
Antibody
Immunogen
Synthetic peptide corresponding to the N-terminal of human MYLPF
Conjugate
Unconjugated
Unconjugated
Unconjugated
Form
Liquid
Concentration
1 mg/mL
Amount
100 µg
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 50% glycerol
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
Product Specific Information
This antibody detects endogenous protein at a molecular weight of 19 kDa.
Purity is >95% by SDS-PAGE.
Target Information
MYLPF (myosin light chain, phosphorylatable, fast skeletal muscle), also known as fast skeletal myosin light chain 2 or MLC2B, is a 169 amino acid protein that is expressed in fetal and adult skeletal muscle. A calcium binding protein, MYLPF contains three EF hand domains and is encoded by a gene that maps to human chromosome 16p11.2. Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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Bioinformatics
Protein Aliases: DKFZp779C0757; DTNB; fast skeletal myosin light chain 2; G2; HUMMLC2B; MGC13450; MLC-2; MLC2F; myosin light chain; myosin light chain 11; myosin light chain 2; myosin light chain, phosphorylatable, fast skeletal muscle; myosin, light chain 11, regulatory; Myosin, light polypeptide 2, alkali; Myosin, light polypeptide 2, alkali; ventricular, skeletal, slow; similar to rabbit skeletal muscle myosin light chain 2; unnamed protein product; ventricular, skeletal, slow
Gene Aliases: 2410014J02Rik; DA1C; HUMMLC2B; MLC-2; MLC2; MLC2B; MRLC2; Myl11; Myl2; MYLPF; Myolc1
UniProt ID: (Human) Q96A32, (Rat) P04466, (Mouse) P97457
Entrez Gene ID: (Human) 29895, (Rat) 24584, (Mouse) 17907
Disclaimer
Clicking the images or links will redirect you to a website hosted by BenchSci that provides third-party scientific content. Neither the content nor the BenchSci technology and processes for selection have been evaluated by us; we are providing them as-is and without warranty of any kind, including for use or application of the Thermo Fisher Scientific products presented.
Performance Guarantee
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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