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Mouse Anti-MYO18B Recombinant Antibody (CBMAB-Z0133-LY)

The product is antibody recognizes MYO18B. The antibody immunoassay techniques such as: IHC-P, FC.
See all MYO18B antibodies

Summary

Host Animal
Mouse
Specificity
Human
Antibody Isotype
IgG
Application
IHC-P, FC

Basic Information

Immunogen
This MYO18B antibody is generated from a mouse immunized with recombinant protein from human MYO18B.
Specificity
Human
Antibody Isotype
IgG
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
Buffer
Purified monoclonal antibody in PBS supplemented with 0.09% (W/V) sodium azide.
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
Myosin XVIIIB
Introduction
The protein encoded by this gene may regulate muscle-specific genes when in the nucleus and may influence intracellular trafficking when in the cytoplasm. The encoded protein functions as a homodimer and may interact with F actin. Mutations in this gene are associated with lung cancer. [provided by RefSeq, Jul 2008]
Entrez Gene ID
UniProt ID
Alternative Names
Unconventional myosin-XVIIIb, MYO18B
Function
May be involved in intracellular trafficking of the muscle cell when in the cytoplasm, whereas entering the nucleus, may be involved in the regulation of muscle specific genes. May play a role in the control of tumor development and progression; restored MYO18B expression in lung cancer cells suppresses anchorage-independent growth.
Biological Process
Cardiac muscle cell development Source: Ensembl
In utero embryonic development Source: Ensembl
Vasculogenesis Source: Ensembl
Cellular Location
Nucleus
Cytoplasm
Other locations
sarcomere
Note: Punctate pattern in undifferentiated myoblasts. Nuclear, on primary cardiomyocytes and adult muscle. A partial sarcomeric location was found in some cardiomyocytes.
Involvement in disease
Klippel-Feil syndrome 4, autosomal recessive, with nemaline myopathy and facial dysmorphism (KFS4):
A form of Klippel-Feil syndrome, a skeletal disorder characterized by congenital fusion of cervical vertebrae. It is due to a failure in the normal segmentation of vertebrae during the early weeks of fetal development. The clinical triad consists of short neck, low posterior hairline, and limited neck movement. KFS4 features additionally include myopathy, mild short stature, microcephaly, and distinctive facies.
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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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