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CAC1F, Polyclonal Antibody

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產(chǎn)品名稱: CAC1F, Polyclonal Antibody
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CAC1F, Polyclonal Antibody


CAC1F, Polyclonal Antibody  的詳細(xì)介紹
Product Name

CAC1F, Polyclonal Antibody

Full Product Name

CAC1F Polyclonal Antibody

Product Synonym Names
Voltage-dependent L-type calcium channel subunit alpha-1F; Voltage-gated calcium channel subunit alpha Cav1.4; CACNA1F; CACNAF1
Product Gene Name

anti-CAC1F antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
300071
3D Structure
ModBase 3D Structure for O60840
Clonality
Polyclonal
Host
Rabbit
Species Reactivity
Human, Mouse
Purity/Purification
Affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Form/Format
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Immunogen
Synthesized peptide derived from human protein. at AA range: 140-220
Preparation and Storage
Store at-20 degree C for 1 year.
Other Notes
Small volumes of anti-CAC1F 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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Applications Tested/Suitable for anti-CAC1F antibody
Western Blot (WB), ELISA (EIA)
Application Notes for anti-CAC1F antibody
WB: 1:500-2000
ELISA: 1:5000-20000
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NCBI/Uniprot data below describe general gene information for CAC1F. It may not necessarily be applicable to this product.
NCBI GI #
377823715
NCBI GeneID
778
NCBI Accession #
NP_001243718.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001256789.2 [Other Products]
UniProt Primary Accession #
O60840 [Other Products]
UniProt Secondary Accession #
O43901; O95226; Q9UHB1; A6NI29; F5CIQ9[Other Products]
UniProt Related Accession #
O60840[Other Products]
Molecular Weight
217
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NCBI Official Full Name
voltage-dependent L-type calcium channel subunit alpha-1F isoform 2
NCBI Official Synonym Full Names
calcium voltage-gated channel subunit alpha1 F
NCBI Official Symbol
CACNA1F??[Similar Products]
NCBI Official Synonym Symbols
JM8; OA2; AIED; COD3; COD4; JMC8; CORDX; CSNB2; CORDX3; CSNB2A; CSNBX2; Cav1.4; Cav1.4alpha1
??[Similar Products]
NCBI Protein Information
voltage-dependent L-type calcium channel subunit alpha-1F
UniProt Protein Name
Voltage-dependent L-type calcium channel subunit alpha-1F
UniProt Synonym Protein Names
Voltage-gated calcium channel subunit alpha Cav1.4
UniProt Gene Name
CACNA1F??[Similar Products]
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NCBI Summary for CAC1F
This gene encodes a multipass transmembrane protein that functions as an alpha-1 subunit of the voltage-dependent calcium channel, which mediates the influx of calcium ions into the cell. The encoded protein forms a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. Mutations in this gene can cause X-linked eye disorders, including congenital stationary night blindness type 2A, cone-rod dystropy, and Aland Island eye disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2013]
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UniProt Comments for CAC1F
Isoform 1: Voltage-sensitive calcium channels (VSCC) mediate the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. The isoform alpha-1F gives rise to L-type calcium currents. Long-lasting (L-type) calcium channels belong to the 'high-voltage activated' (HVA) group. They are blocked by dihydropyridines (DHP), phenylalkylamines, benzothiazepines, and by omega-agatoxin-IIIA (omega-Aga-IIIA). They are however insensitive to omega-conotoxin-GVIA (omega-CTx-GVIA) and omega-agatoxin-IVA (omega-Aga-IVA). Activates at more negative voltages and does not undergo calcium-dependent inactivation (CDI), due to incoming calcium ions, during depolarization.
Research Articles on CAC1F
1. These two cases demonstrate the clinical overlap between Leber congenital amaurosis and type 2 congenital stationary night blindness in infants and young children. Genetic testing is an essential tool in these cases and provides a more accurate diagnosis and prognosis for patients with inherited retinal degenerative disorders.
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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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