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簡要描述:Proteus BioSciences 代理,Proteus BioSciences 中國,Proteus BioSciences 代理,Proteus BioSciences 公司,Proteus BioSciences 專業(yè)代理-上海起發(fā)實(shí)驗(yàn)試劑有限公司,具體產(chǎn)品信息歡迎電詢:4006551678

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  • 更新時間:2025-06-04
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世界*實(shí)驗(yàn)材料供應(yīng)商Proteus BioSciences 正式授權(quán)上海起發(fā)為其中國代理,Proteus BioSciences  在一直是行業(yè)的*,一直為廣大科研客戶提供zui為優(yōu)質(zhì)的產(chǎn)品和服務(wù),上海起發(fā)一直秉承為中國科研客戶帶來的產(chǎn)品,的服務(wù), 簽約Proteus BioSciences  就是為了給廣大科研客戶帶來更加完善的產(chǎn)品和服務(wù),您的滿意將是我們zui大的收獲

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加拿大Proteus BioSciences  www.proteus-biosciences。。com
Proteus BioSciences was founded in 2002 to develop innovative products to advance proteomic research. We specialize in discovering peptides and proteins with novel biological properties, designing and developing enzyme activity assays for diverse screening applications, and producing innovative protein analysis tools for biomarker identification and characterization.

With extensive research and product development expertise, academic and industrial biotechnology experience, and a solid business development and technology licensing track record, our efforts have contributed to the the publication of hundreds of peer-reviewed scientific articles and the development of thousands of life science research products. These products support studies in numerous fields including biochemistry, cell and molecular biology, genetics, immunology, neuroscience, and virology. We established and continue to collaborate with a network of over 500 scientific investigators worldwide and we intend to continue encouraging these relationships in the future to improve life science, biomedical and health care research.

 Proteus BioSciences was founded in 2002 to discover peptides and proteins with novel biological properties, design and develop enzyme activity assays for diverse screening applications, and produce innovative protein analysis tools. Proteus BioSciences’ products support research in such diverse fields as biochemistry, cell & molecular biology, genetics, immunology, neuroscience and virology.

The Proteus BioSciences product range includes:

Antibodies 
Enzyme activity assays 
Proteins 
Protein analysis 
Services offered include production of polyclonal antisera, immunochemistry and purification of fusion-tagged protein.

Myosin-VIIa

Rabbit Polyclonal Antibody

PRODUCT #: 25-6790


DESCRIPTION: Myosin-VIIa is one of the unconventional members of the myosin molecular motor superfamily that move along filamentous actin. The protein is expressed primarily in the inner ear, retina and testis. Defects in the myosin-VIIa gene (MYO7A) are responsible for Usher syndrome, characterized by hearing impairment, lack of vestibular function and progressive retinal degeneration.MYO7A mutations are are responsible for deafness in shaker-1 mice and in other model systems. In the inner ear, myosin-VIIa is required for assembly of stereocilia, the sensory structures necessary for detecting sound signals. 

SPECIES CROSS-REACTIVITY:

Human, mouse, rat, pig, avian, amphibian

APPLICATIONS/DILUTIONS:

IF (5-10 ug/ml)
WB (0.5-1.0 ug/ml)

SOURCE:

Rabbits were immunized with amino acids 880-1077 from the tail region of human myosin-VIIa.

FORM/STORAGE:

50 ug (0.5 mg/ml) of affinity purified IgG with 50% glycerol, 0.01% sodium azide and 1.0 mg/ml BSA.  Store at -20o C.  Avoid multiple freeze/thaw cycles.

References:
Hasson, T. et al. (1995), Proc. Natl. Acad. Sci. 92:9815-9819.
Hasson, T. et al. (1997), Journal of Cell Biology 137:1287-1307. 
Hasson, T. et al. (1997), Cell Motil. Cytoskel. 37:127-138.
Hasson, T. et al. (2005), Cell Motil. Cytoskel. 62:13-26.

DESCRIPTION: Myosin-VIIa is one of the unconventional members of the myosin molecular motor superfamily that move along filamentous actin. The protein is expressed primarily in the inner ear, retina and testis. Defects in the myosin-VIIa gene (MYO7A) are responsible for Usher syndrome, characterized by hearing impairment, lack of vestibular function and progressive retinal degeneration.MYO7A mutations are are responsible for deafness in shaker-1 mice and in other model systems. In the inner ear, myosin-VIIa is required for assembly of stereocilia, the sensory structures necessary for detecting sound signals. 
 

SPECIES CROSS-REACTIVITY:

Human, mouse, rat, pig, avian, amphibian
 

APPLICATIONS/DILUTIONS:

IF (5-10 ug/ml)
WB (0.5-1.0 ug/ml)
 

SOURCE:

Rabbits were immunized with amino acids 880-1077 from the tail region of human myosin-VIIa.
 

FORM/STORAGE:

50 ug (0.5 mg/ml) of affinity purified IgG with 50% glycerol, 0.01% sodium azide and 1.0 mg/ml BSA.  Store at -20o C.  Avoid multiple freeze/thaw cycles.
 

References:
Hasson, T. et al. (1995), Proc. Natl. Acad. Sci. 92:9815-9819.
Hasson, T. et al. (1997), Journal of Cell Biology 137:1287-1307. 
Hasson, T. et al. (1997), Cell Motil. Cytoskel. 37:127-138.
Hasson, T. et al. (2005), Cell Motil. Cytoskel. 62:13-26.

DESCRIPTION: Myosin-VIIa is one of the unconventional members of the myosin molecular motor superfamily that move along filamentous actin. The protein is expressed primarily in the inner ear, retina and testis. Defects in the myosin-VIIa gene (MYO7A) are responsible for Usher syndrome, characterized by hearing impairment, lack of vestibular function and progressive retinal degeneration.MYO7A mutations are are responsible for deafness in shaker-1 mice and in other model systems. In the inner ear, myosin-VIIa is required for assembly of stereocilia, the sensory structures necessary for detecting sound signals. 

SPECIES CROSS-REACTIVITY:

Human, mouse, rat, pig, avian, amphibian

APPLICATIONS/DILUTIONS:

IF (5-10 ug/ml)
WB (0.5-1.0 ug/ml)

SOURCE:

Rabbits were immunized with amino acids 880-1077 from the tail region of human myosin-VIIa.

FORM/STORAGE:

50 ug (0.5 mg/ml) of affinity purified IgG with 50% glycerol, 0.01% sodium azide and 1.0 mg/ml BSA.  Store at -20o C.  Avoid multiple freeze/thaw cycles.

References:
Hasson, T. et al. (1995), Proc. Natl. Acad. Sci. 92:9815-9819.
Hasson, T. et al. (1997), Journal of Cell Biology 137:1287-1307. 
Hasson, T. et al. (1997), Cell Motil. Cytoskel. 37:127-138.
Hasson, T. et al. (2005), Cell Motil. Cytoskel. 62:13-26.




DESCRIPTION: Myosin-VIIa is one of the unconventional members of the myosin molecular motor superfamily that move along filamentous actin. The protein is expressed primarily in the inner ear, retina and testis. Defects in the myosin-VIIa gene (MYO7A) are responsible for Usher syndrome, characterized by hearing impairment, lack of vestibular function and progressive retinal degeneration.MYO7A mutations are are responsible for deafness in shaker-1 mice and in other model systems. In the inner ear, myosin-VIIa is required for assembly of stereocilia, the sensory structures necessary for detecting sound signals. 

SPECIES CROSS-REACTIVITY:

Human, mouse, rat, pig, avian, amphibian

APPLICATIONS/DILUTIONS:

IF (5-10 ug/ml)
WB (0.5-1.0 ug/ml)

SOURCE:

Rabbits were immunized with amino acids 880-1077 from the tail region of human myosin-VIIa.

FORM/STORAGE:

50 ug (0.5 mg/ml) of affinity purified IgG with 50% glycerol, 0.01% sodium azide and 1.0 mg/ml BSA.  Store at -20o C.  Avoid multiple freeze/thaw cycles.

References:
Hasson, T. et al. (1995), Proc. Natl. Acad. Sci. 92:9815-9819.
Hasson, T. et al. (1997), Journal of Cell Biology 137:1287-1307. 
Hasson, T. et al. (1997), Cell Motil. Cytoskel. 37:127-138.
Hasson, T. et al. (2005), Cell Motil. Cytoskel. 62:13-26.

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