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Key Documents

SAB3500487

Sigma-Aldrich

Anti-SAE2 antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

Synonym(s):

Anti-ARX, Anti-SUMO1 activating enzyme subunit 2, Anti-UBA2, Anti-ubiquitin-like modifier activating enzyme 2

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100 μG
$540.00

$540.00

Usually ships in 5 business days. (Orders outside of US, please allow an additional 1-2 weeks for delivery)
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100 μG
$540.00

About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

$540.00

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

biological source

rabbit

Quality Level

100

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

human

technique(s)

immunocytochemistry: suitable
immunofluorescence: suitable
indirect ELISA: suitable
western blot: suitable

NCBI accession no.

NP_005490

UniProt accession no.

Q9UBT2

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... UBA2(10054)

Immunogen

SAE2 antibody was raised against an 18 amino acid peptide near the carboxy terminus of human SAE2.

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.

Linkage

The action of this antibody can be blocked using blocking peptide SBP3500487.

Physical form

Supplied in PBS with 0.02% sodium azide.

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Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
57511002

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Gretchen L Bentz et al.
PloS one, 14(5), e0217578-e0217578 (2019-05-28)
Cellular sumoylation processes are proposed targets for anti-viral and anti-cancer therapies. We reported that Epstein-Barr virus (EBV) latent membrane protein 1 (LMP1) dysregulates cellular sumoylation processes, contributing to its oncogenic potential in EBV-associated malignancies. Ginkgolic acid and anacardic acid, known

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