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Merck
CN

SAB2501893

Anti-SYNGAP1 (N-terminal) antibody produced in goat

affinity isolated antibody, buffered aqueous solution

Synonym(s):

DKFZp761G1421, KIAA1938, MRD5, synaptic Ras GTPase activating protein 1

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About This Item

NACRES:
NA.41
UNSPSC Code:
12352203
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Product Name

Anti-SYNGAP1 (N-terminal) 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

bovine, rat, canine, pig, mouse, human

technique(s)

indirect ELISA: suitable
western blot: suitable

UniProt accession no.

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... SYNGAP1(8831)

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.

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.

Immunogen

Peptide with sequence DEDEIHPLLIRDR-C, from the N-terminal region of the protein sequence according toNP_006763.2

Physical form

Supplied at 0.5 mg/mL in 20mM Tris (pH 7.3) and 150mM NaCl with 0.02% sodium azide and 0.5% bovine serum albumin.

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Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Yudong Gao et al.
Nature communications, 15(1), 6801-6801 (2024-08-10)
One of the main drivers of autism spectrum disorder is risk alleles within hundreds of genes, which may interact within shared but unknown protein complexes. Here we develop a scalable genome-editing-mediated approach to target 14 high-confidence autism risk genes within
Yoichi Araki et al.
Proceedings of the National Academy of Sciences of the United States of America, 120(37), e2308891120-e2308891120 (2023-09-05)
SYNGAP1 is a Ras-GTPase-activating protein highly enriched at excitatory synapses in the brain. De novo loss-of-function mutations in SYNGAP1 are a major cause of genetically defined neurodevelopmental disorders (NDDs). These mutations are highly penetrant and cause SYNGAP1-related intellectual disability (SRID)

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