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SAE1 Rabbit Polyclonal Antibody

SAE1 Rabbit Polyclonal Antibody

Catalog Number: S0B60415 Application: WB, IHC-P, ICC Reactivity: Hu, Mk Conjugation: Unconjugated Brand: Starter
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Regular price $100 USD
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Product Details

Product Specification


Host Rabbit
Antigen SAE1
Synonyms SUMO-activating enzyme subunit 1; AOS1; SUA1; UBLE1A
Immunogen Synthetic Peptide
Location Nucleus
Accession Q9UBE0
Antibody Type Polyclonal antibody
Isotype IgG
Application WB, IHC-P, ICC
Reactivity Hu, Mk
Positive Sample HEK-293, HeLa, Jurkat, MCF7, COS7
Purification Immunogen Affinity
Concentration 2 mg/ml
Conjugation Unconjugated
Physical Appearance Liquid
Storage Buffer

PBS, 40% Glycerol, 0.05% BSA, 0.02% sodium azide

Stability & Storage

12 months from date of receipt / reconstitution, -20 °C as supplied

Dilution


application dilution species
WB 1:1000 Hu, Mk
IHC-P 1:800 Hu
ICC 1:400 Hu

Background

SAE1 is a key component in the SUMOylation modification cascade. It forms a heterodimeric complex (SAE1/SAE2) with SAE2 protein, functioning as the E1 activating enzyme to catalyze the activation of SUMO molecules (such as SUMO1, SUMO2/3) in the presence of ATP, and subsequently transfers SUMO to the E2 conjugating enzyme UBC9 through a transesterification reaction, thereby initiating the entire SUMO modification process. This protein consists of 346 amino acids with a molecular weight of approximately 40 kDa, and contains a critical cysteine residue (Cys-173) that is responsible for forming a high-energy thioester bond intermediate with SUMO during catalysis. SAE1 is highly conserved across eukaryotes and is essential for numerous fundamental biological processes, including cell cycle regulation, DNA damage repair, transcriptional regulation, and nucleocytoplasmic transport. Interestingly, although SAE1 is essential for SUMOylation, its expression level in human cancers exhibits a bidirectional correlation with prognosis—for example, high SAE1 expression indicates poor prognosis in bladder cancer, whereas high expression in lung or renal cancer is associated with better survival outcomes, suggesting that its impact on tumors is tissue-specific. Furthermore, the involvement of SAE1 in various diseases is being progressively uncovered, including its role in promoting viral replication through HBV-induced SUMOylation of SAE1, its participation in ovarian cancer metastasis and drug resistance, and the potential association of its gene polymorphisms with the risk of spontaneous preterm birth, making it a potential disease biomarker and therapeutic target.

Picture

Western Blot

WB result of SAE1 Rabbit pAb
Primary antibody: SAE1 Rabbit pAb at 1/1000 dilution
Lane 1: HEK-293 whole cell lysate 20 µg
Lane 2: Hela whole cell lysate 20 µg
Lane 3: Jurkat whole cell lysate 20 µg
Lane 4: MCF7 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 38 kDa
Observed MW: 38 kDa

WB result of SAE1 Rabbit pAb
Primary antibody: SAE1 Rabbit pAb at 1/1000 dilution
Lane 1: COS7 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 38 kDa
Observed MW: 38 kDa

Immunohistochemistry

IHC shows positive staining in paraffin-embedded human colon. Anti-SAE1 antibody was used at 1/800 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded human testis. Anti-SAE1 antibody was used at 1/800 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

Immunocytochemistry

ICC shows positive staining in HeLa cells. Anti- SAE1 antibody was used at 1/400 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).