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MYO1A, Polyclonal Antibody

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产品名称: MYO1A, Polyclonal Antibody
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简单介绍

MYO1A, Polyclonal Antibody


MYO1A, Polyclonal Antibody  的详细介绍
Product Name

MYO1A, Polyclonal Antibody

Full Product Name

MYO1A Antibody - middle region

Product Gene Name

anti-MYO1A antibody

[Similar Products]
Product Synonym Gene Name
BBMI; MIHC; MYHL; DFNA48[Similar Products]
Antibody/Peptide Pairs
MYO1A peptide (MBS3245694) is used for blocking the activity of MYO1A antibody (MBS3220897)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Immunogen Sequence
Synthetic peptide located within the following region: ILEDNSFEQF VINYCNEKLQ QVFIEMTLKE EQEEYKREGI PWTKVDYFDN
OMIM
601478
3D Structure
ModBase 3D Structure for Q9UBC5
Clonality
Polyclonal
Host
Rabbit
Species Reactivity
Human
Purity/Purification
Affinity purified
Form/Format
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Immunogen
The immunogen is a synthetic peptide directed towards the middle region of human MYO1A
Preparation and Storage
For short term use, store at 2-8 degree C up to 1 week. For long term storage, store at -20 degree C in small aliquots to prevent freeze-thaw cycles.
Other Notes
Small volumes of anti-MYO1A antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
anti-MYO1A antibody
This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with autosomal dominant deafness. Alternatively spliced variants have been found for this gene.
Product Categories/Family for anti-MYO1A antibody
Polyclonal; Developmental Biology; Membrane & Traffic; Disease Related; Meiosis/Mitosis/Cell Cycle;
Applications Tested/Suitable for anti-MYO1A antibody
Western Blot (WB)

Western Blot (WB) of anti-MYO1A antibody
Host: Rabbit
Target Name: MYO1A
Sample Tissue: Human THP-1 Whole Cell lysates
Antibody Dilution: 1ug/ml
anti-MYO1A antibody Western Blot (WB) (WB) image
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NCBI/Uniprot data below describe general gene information for MYO1A. It may not necessarily be applicable to this product.
NCBI GI #
365733629
NCBI GeneID
4640
NCBI Accession #
NP_001242970.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001256041.1 [Other Products]
UniProt Primary Accession #
Q9UBC5 [Other Products]
UniProt Related Accession #
Q9UBC5[Other Products]
Molecular Weight
115 kDa
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NCBI Official Full Name
unconventional myosin-Ia
NCBI Official Synonym Full Names
myosin IA
NCBI Official Symbol
MYO1A  [Similar Products]
NCBI Official Synonym Symbols
BBMI; MIHC; MYHL; DFNA48
  [Similar Products]
NCBI Protein Information
unconventional myosin-Ia
UniProt Protein Name
Unconventional myosin-Ia
UniProt Synonym Protein Names
Brush border myosin I; BBM-I; BBMI; Myosin I heavy chain; MIHC
Protein Family
Unconventional myosin
UniProt Gene Name
MYO1A  [Similar Products]
UniProt Synonym Gene Names
MYHL; BBM-I; BBMI; MIHC  [Similar Products]
UniProt Entry Name
MYO1A_HUMAN
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NCBI Summary for MYO1A
This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with autosomal dominant deafness. Alternatively spliced variants have been found for this gene. [provided by RefSeq, Dec 2011]
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Research Articles on MYO1A
1. These data do not support a causal relationship of variants in MYO1A to sensorineural hearing loss. We suggest that the genotypic ascertainment method is useful to objectively evaluate gene-phenotype associations.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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