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ACTB, Blocking Peptide

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产品名称: ACTB, Blocking Peptide
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简单介绍

ACTB, Blocking Peptide


ACTB, Blocking Peptide  的详细介绍
Product Name

ACTB, Blocking Peptide

Full Product Name

ACTB Peptide - N-terminal region

Product Gene Name

ACTB blocking peptide

[Similar Products]
Product Synonym Gene Name
BRWS1; PS1TP5BP1; ACTB[Similar Products]
Antibody/Peptide Pairs
ACTB peptide (MBS3246510) is used for blocking the activity of ACTB antibody (MBS3221784)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Sequence
Synthetic peptide located within the following region: EEEIAALVID NGSGMCKAGF AGDDAPRAVF PSIVGRPRHQ GVMVGMGQKD
OMIM
phenotype 614583
3D Structure
ModBase 3D Structure for P63261
Species Reactivity
Human
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of ACTB blocking peptide 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
ACTB blocking peptide
This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins that are ubiquitously expressed. Mutations in this gene cause Baraitser-Winter syndrome 1, which is characterized by intellectual disability with a distinctive facial appearance in human patients. Numerous pseudogenes of this gene have been identified throughout the human genome.
Product Categories/Family for ACTB blocking peptide
Peptide
NCBI/Uniprot data below describe general gene information for ACTB. It may not necessarily be applicable to this product.
NCBI GI #
316659409
NCBI GeneID
71
NCBI Accession #
NP_001186883.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001199954.1 [Other Products]
UniProt Primary Accession #
P63261 [Other Products]
UniProt Related Accession #
P63261[Other Products]
Molecular Weight
41 kDa
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NCBI Official Full Name
actin, cytoplasmic 2
NCBI Official Synonym Full Names
actin gamma 1
NCBI Official Symbol
ACTG1  [Similar Products]
NCBI Official Synonym Symbols
ACT; ACTG; DFNA20; DFNA26; HEL-176
  [Similar Products]
NCBI Protein Information
actin, cytoplasmic 2
UniProt Protein Name
Actin, cytoplasmic 2
UniProt Synonym Protein Names
Gamma-actinActin, cytoplasmic 2, N-terminally processed
Protein Family
Actin
UniProt Gene Name
ACTG1  [Similar Products]
UniProt Synonym Gene Names
ACTG  [Similar Products]
UniProt Entry Name
ACTG_HUMAN
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NCBI Summary for ACTB
Actins are highly conserved proteins that are involved in various types of cell motility and in maintenance of the cytoskeleton. Three main groups of actin isoforms have been identified in vertebrate animals: alpha, beta, and gamma. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton and as mediators of internal cell motility. Actin gamma 1, encoded by this gene, is a cytoplasmic actin found in all cell types. Mutations in this gene are associated with DFNA20/26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss and also with Baraitser-Winter syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]
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UniProt Comments for ACTB
ACTG1: Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to 4 others. Belongs to the actin family.

Protein type: Motility/polarity/chemotaxis; Cytoskeletal

Chromosomal Location of Human Ortholog: 17q25

Cellular Component: filamentous actin; extracellular space; cytoskeleton; myofibril; membrane; plasma membrane; nucleus; cytosol

Molecular Function: identical protein binding; protein binding; structural constituent of cytoskeleton; ubiquitin protein ligase binding; ATP binding

Biological Process: axon guidance; retinal homeostasis; intercellular junction assembly and maintenance; ephrin receptor signaling pathway; innate immune response; sarcomere organization; cell motility; vascular endothelial growth factor receptor signaling pathway

Disease: Baraitser-winter Syndrome 2; Deafness, Autosomal Dominant 20
Research Articles on ACTB
1. A novel actin gamma 1 (ACTG1) de novo mutation is identified in two sporadic, juvenile, Chinese non-syndromic hearing loss (NSHL) cases using targeted high-throughput sequencing.
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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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