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Mouse Anti-MYLPF Recombinant Antibody (CBXF-1961) (CBMAB-F2800-CQ)

This product is a mouse antibody that recognizes MYLPF. The antibody CBXF-1961 can be used for immunoassay techniques such as: WB, IHC-P.
See all MYLPF antibodies

Summary

Host Animal
Mouse
Specificity
Rat, Human
Clone
CBXF-1961
Antibody Isotype
IgG1
Application
WB, IHC-P

Basic Information

Specificity
Rat, Human
Antibody Isotype
IgG1
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Concentration
1 mg/mL
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
fast skeletal myosin light chain 2
Introduction
MYLPF (Myosin Light Chain, Phosphorylatable, Fast Skeletal Muscle) is a Protein Coding gene. Among its related pathways are Cardiac conduction and PAK Pathway. Gene Ontology (GO) annotations related to this gene include calcium ion binding and structural constituent of muscle. An important paralog of this gene is MYL10.
Entrez Gene ID
Human29895
Rat24584
UniProt ID
HumanQ96A32
RatP04466
Alternative Names
Myosin Light Chain, Phosphorylatable, Fast Skeletal Muscle; Myosin, Light Chain 11, Regulatory; Fast Skeletal Myosin Light Chain 2; MLC2B; Myosin Regulatory Light Chain 2, Skeletal Muscle Isoform; Myosin Regulatory Light Chain 2;
Function
Plays a role in muscle contraction.
Biological Process
Actin-myosin filament sliding Source: UniProtKB
Immune response Source: Ensembl
Muscle contraction Source: UniProtKB
Muscle tissue morphogenesis Source: UniProtKB
Skeletal muscle tissue development Source: BHF-UCL
Cellular Location
Cytoskeleton
muscle myosin complex
Cytosol
Lysosome
lysosomal membrane
Other locations
cytoplasm
Involvement in disease
Arthrogryposis, distal, 1C (DA1C):
A form of distal arthrogryposis, a disease characterized by congenital joint contractures that mainly involve two or more distal parts of the limbs, in the absence of a primary neurological or muscle disease. DA1C patients show multiple congenital contractures, scoliosis, short stature, and segmental amyoplasia. DA1C inheritance can be autosomal recessive or autosomal dominant.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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