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Merck

S4813

Anti-α1-Syntrophin (RA-16) antibody produced in rabbit

buffered aqueous solution, IgG fraction of antiserum

Synonim(y):

Anti-SNTA1

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Informacje o tej pozycji

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
Conjugate:
unconjugated
Clone:
polyclonal
Application:
ARR, IHC (f), WB
Citations:
8
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biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

IgG fraction of antiserum

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen 60 kDa

species reactivity

rat

technique(s)

immunohistochemistry (frozen sections): suitable using 0.5% paraformaldehyde fixed/0.5% Triton X-100 treated rat skeletal muscle, microarray: suitable, western blot: 1:2,000 using rat skeletal muscle homogenate extract (membrane fraction)

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

mouse ... Snta1(20648)
rat ... Snta1(362242)

General description

α1-syntrophin (SNTA1) is a dystrophin-associated protein, that has four domains- a postsynaptic density protein-95/disc large/zona occludens-1 (PDZ) domain, two pleckstrin homology (PH1 and PH2) domains and a syntrophin unique (SU) domain. It is located on human chromosome 20q11.2. It is usually present in the peripheral cytoplasmic membrane.
Anti-α1-Syntrophin (RA-16) is developed in rabbit using a synthetic peptide corresponding to a sequence of mouse α1-syntrophin The syntrophins are a family of intracellular peripheral membrane proteins (58-60 kDa), comprising at least three isoforms α1, β1, and β2-syntrophins. Syntrophins in mammalian skeletal muscle have been shown to be part of a complex of proteins associated with dystrophin, the product of Duchenne/Becker muscular dystrophy gene. The C-terminal 57 amino acids region of syntrophins is highly conserved among the three isoforms, and may contain the binding site for dystrophin.

Immunogen

synthetic peptide corresponding to a sequence of mouse α1-syntrophin (amino acids 191-206 with N-terminally added lysine) conjugated to KLH.

Application

Anti-α1-Syntrophin (RA-16) antibody produced in rabbit has been used in immunohistochemistry and immunoblotting.

Biochem/physiol Actions

α1-Syntrophin recruit signaling proteins(2) to the membrane via association with the dystrophin complex.
α1-syntrophin (SNTA1) mutations results in LQTS (cardiac channelopathies like long QT syndrome). It modulates the development of adipocyte lipid droplet. It also participates in the survival signaling pathway in myoblasts. α1-syntrophin controls voltage-gated Na+ channels. It acts as a substrate for stress-activated protein kinase-3 (SAPK-3).

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Klasa składowania

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Clinical utility gene card for: long-QT syndrome (types 1-13)
Beckmann BM, et al.
European Journal of Human Genetics, 21(10) (2013)
Role of SNTA1 in Rac1 activation, modulation of ROS generation, and migratory potential of human breast cancer cells
Bhat HF, et al.
British Journal of Cancer, 110(3), 706-714 (2014)
Dystrophin 71 and alpha1syntrophin in morpho-functional plasticity of rat supraoptic nuclei: Effect of saline surcharge and reversibly normal hydration
Sifi M, et al.
Acta Histochemica, 120(3), 187-195 (2018)
?1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium Current
Choi JI, et al.
PLoS ONE, 11(3) (2016)
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current
Cheng J, et al.
Circulation. Arrhythmia and Electrophysiology, 2(6), 667-676 (2009)

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Numer pozycji handlu globalnego

SKUNUMER GTIN
S4813-.2ML04061837724473

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