SAB2500236

Anti-Choline Acetyltransferase Antibody

Name: Anti-Choline Acetyltransferase Antibody
Brand: SIGMA
Price: 584 EUR

goat polyclonal

Synonym(s):

Anti-Acetyl CoA:choline O-acetyltransferase, Anti-CHAT, Anti-CMS1A, Anti-CMS1A2

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100 μG

€584.00

Ships within 5 business days. (Orders outside of US, please allow an additional 1-2 weeks for delivery)

About This Item

MDL number:

MFCD01321843

UNSPSC Code:

12352203

NACRES:

NA.41

Key Documents

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Product Name

Anti-Choline acetyltransferase antibody produced in goat, affinity isolated antibody, buffered aqueous solution

biological source

goat

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

canine, chimpanzee, human, pig

technique(s)

indirect ELISA: suitable
western blot: suitable

UniProt accession no.

P28329

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... CHAT(1103)

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Show Differences

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This Item	AMAB91130	SAB2108655	AMAB91129
Sigma-Aldrich SAB2500236 Anti-Choline acetyltransferase antibody produced in goat	Sigma-Aldrich AMAB91130 Monoclonal Anti-CHAT antibody produced in mouse	Sigma-Aldrich SAB2108655 Anti-CHAT	Sigma-Aldrich AMAB91129 Monoclonal Anti-CHAT antibody produced in mouse
Quality Level 100	Quality Level 100	Quality Level 100	Quality Level 100
conjugate unconjugated	conjugate unconjugated	conjugate unconjugated	conjugate unconjugated
antibody form affinity isolated antibody	antibody form purified immunoglobulin	antibody form affinity isolated antibody	antibody form purified immunoglobulin
biological source goat	biological source mouse	biological source rabbit	biological source mouse
species reactivity canine, chimpanzee, human, pig	species reactivity mouse, human, rat	species reactivity dog, human, horse	species reactivity mouse, rat, human
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. −20°C

General description

Choline acetyltransferase (CHAT) has a molecular weight of about 68kDa. It is synthesized in the parakaryon and is transported to the axon terminals. CHAT is part of the choline/carnitine acyltransferase family.

Immunogen

Peptide with sequence CKEKATRPSQGHQP from the C Terminus of the protein sequence according to NP_065574; NP_066264; NP_066265; NP_066266.

Biochem/physiol Actions

Choline acetyltransferase (CHAT) is involved in the synthesis of acetylcholine in neurons. It catalyzes the transfer of an acetyl group between acetyl-coenzyme A and choline. Mutations in the gene encoding this protein have been associated with congenital neuromuscular disorders.

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

Supplied at 0.5 mg/mL in Tris saline with 0.02% sodium azide and 0.5% bovine serum albumin.

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 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number

6636P1

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Blood pressure regulation by CD4+ lymphocytes expressing choline acetyltransferase.

Olofsson PS, e.al

Nature Biotechnology (2016)

Choline acetyltransferase structure reveals distribution of mutations that cause motor disorders

The Embo Journal (2004)

Loss of PML nuclear bodies in familial amyotrophic lateral sclerosis-frontotemporal dementia.

Francesco Antoniani et al.

Cell death discovery, 9(1), 248-248 (2023-07-16)

Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) are two neurodegenerative disorders that share genetic causes and pathogenic mechanisms. The critical genetic players of ALS and FTD are the TARDBP, FUS and C9orf72 genes, whose protein products, TDP-43, FUS and

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