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Key Documents

SAB5200036

Sigma-Aldrich

Monoclonal Anti-KCNT1 antibody produced in mouse

clone S3-26, 1 mg/mL, purified immunoglobulin

Synonym(s):

Anti-SLACK potassium channel, S3-26, Anti-potassium channel, subfamily T, member 1

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

mouse

Quality Level

100

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

S3-26, monoclonal

form

buffered aqueous glycerol solution

mol wt

antigen predicted mol wt 140 kDa

species reactivity

rat, human (weak), mouse

concentration

1 mg/mL

technique(s)

immunohistochemistry: suitable
western blot: suitable

isotype

IgG1

NCBI accession no.

NP_068625

UniProt accession no.

Q5JUK3

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

rat ... Kcnt1(60444)

Specificity

Detects ~140 kDa.

Immunogen

Fusion protein amino acids 1168-1237 of rat Slo2.2 (Slack); NP_068625

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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Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Duyen H Pham et al.
Human molecular genetics, 26(11), 2042-2052 (2017-03-24)
De novo and inherited mutations of X-chromosome cell adhesion molecule protocadherin 19 (PCDH19) cause frequent, highly variable epilepsy, autism, cognitive decline and behavioural problems syndrome. Intriguingly, hemizygous null males are not affected while heterozygous females are, contradicting established X-chromosome inheritance.

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