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SAB5200059

Monoclonal Anti-KCNA2 antibody produced in mouse

clone S14-16, 1 mg/mL, purified immunoglobulin

Synonyme(s) :

Anti-HBK5, Anti-HUKIV, Anti-Kca12, Anti-Kv1.2 K+ channel, S14-16, Anti-MK2, Anti-NGK1

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A propos de cet article

NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
S14-16, monoclonal
Application:
IHC, IP, WB
Citations:
1
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biological source

mouse

Quality Level

100

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

S14-16, monoclonal

form

buffered aqueous glycerol solution

mol wt

antigen predicted mol wt 80 kDa

species reactivity

human, rat, mouse, zebrafish

concentration

1 mg/mL

technique(s)

immunohistochemistry: suitable, immunoprecipitation (IP): suitable, western blot: suitable

isotype

IgG2b

NCBI accession no.

NP_032443.3

UniProt accession no.

P16389

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... KCNA2(3737)
mouse ... Kcna2(16490)

Immunogen

Fusion protein amino acids 428-499 (cytoplasmic C-terminus) of rat Kv1.2

Biochem/physiol Actions

Detects ~80 kDa

Features and Benefits

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Physical form

Solution in PBS, pH 7.4, 50% glycerol, and 0.09% 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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Classe de stockage

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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Consulter la Bibliothèque de documents

Kevin L Seburn et al.
Journal of neuropathology and experimental neurology, 73(7), 693-701 (2014-06-12)
Mutations in HINT1, the gene encoding histidine triad nucleotide-binding protein 1 (HINT1), cause a recessively inherited peripheral neuropathy that primarily involves motor dysfunction and is usually associated with neuromyotonia (i.e. prolonged muscle contraction resulting from hyperexcitability of peripheral nerves). Because

Numéro d'article de commerce international

RéférenceGTIN
SAB5200059-100UG04061838058829