ESCO2 Polyclonal antibody

ESCO2 Polyclonal Antibody for WB, IHC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IHC, ELISA

Conjugate

Unconjugated

Cat no : 23525-1-AP

Synonyms

N acetyltransferase ESCO2, hEFO2, Establishment factor-like protein 2, EFO2p, EFO2


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Tested Applications

Positive WB detected inHeLa cells, HepG2 cells, mouse testis, rat testis
Positive IHC detected inhuman skin cancer tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:3000
Immunohistochemistry (IHC)IHC : 1:150-1:600
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Published Applications

WBSee 2 publications below

Product Information

23525-1-AP targets ESCO2 in WB, IHC, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Cited Reactivityhuman
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen ESCO2 fusion protein Ag18893 相同性解析による交差性が予測される生物種
Full Name establishment of cohesion 1 homolog 2 (S. cerevisiae)
Calculated molecular weight 601 aa, 68 kDa
Observed molecular weight 65-70 kDa
GenBank accession numberBC146562
Gene symbol ESCO2
Gene ID (NCBI) 157570
RRIDAB_2879292
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen Affinity purified
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

ESCO2 is also known as Establishment of Sister Chromatid Cohesion N-Acetyltransferase 2, EFO2. This gene encodes a member of the family of acetyltransferases involved in the establishment of sister chromatid cohesion during S phase and postreplicative sister chromatid cohesion induced by double-strand breaks (PubMed: 15821733). Mutations in the ESCO2 gene are associated with a rare genetic disorder called Roberts syndrome or SC phocomelia syndrome (PubMed: 16380922). The loss of function or impaired activity of the ESCO2 protein due to mutations disrupts the proper cohesion of sister chromatids, leading to chromosomal abnormalities and the characteristic features of Roberts syndrome. ESCO2 can be detected as about 65-70 kDa.

Protocols

Product Specific Protocols
WB protocol for ESCO2 antibody 23525-1-APDownload protocol
IHC protocol for ESCO2 antibody 23525-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

Kaohsiung J Med Sci

Long noncoding RNA ZFPM2-AS1 regulates renal cell carcinoma progression via miR-130a-3p/ESCO2.

Authors - Gang Zhang
humanWB

BMC Cancer

ESCO2's oncogenic role in human tumors: a pan-cancer analysis and experimental validation

Authors - Yue Huang