製品: OBFC2A Antibody
カタログ: DF12433
タンパク質の説明: Rabbit polyclonal antibody to OBFC2A
アプリケーション: WB IHC IF/ICC
Cited expt.: WB
反応性: Human
予測: Pig, Bovine, Horse, Sheep, Rabbit, Dog
分子量: 22 kDa; 22kD(Calculated).
ユニプロット: Q96AH0
RRID: AB_2845238

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製品説明

ソース:
Rabbit
アプリケーション:
WB 1:500-1:2000, IHC 1:50-1:200, IF/ICC 1:100-1:500
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*Tips:

WB: For western blot detection of denatured protein samples. IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.

反応性:
Human
予測:
Pig(92%), Bovine(86%), Horse(92%), Sheep(86%), Rabbit(100%), Dog(92%)
クローナリティ:
Polyclonal
特異性:
OBFC2A Antibody detects endogenous levels of total OBFC2A.
RRID:
AB_2845238
引用形式: Affinity Biosciences Cat# DF12433, RRID:AB_2845238.
コンジュゲート:
Unconjugated.
精製:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
別名:

折りたたみ/展開

FLJ13624; FLJ22833; hSSB2; MGC111163; Nabp1; Nucleic acid-binding protein 1; OBFC2A; Oligonucleotide/oligosaccharide binding fold containing 2A; Oligonucleotide/oligosaccharide binding fold containing protein 2A; Oligonucleotide/oligosaccharide-binding fold-containing protein 2A; Sensor of single strand DNA complex subunit B2; Sensor of single-strand DNA complex subunit B2; Sensor of ssDNA subunit B2; Single stranded DNA binding protein 2; Single-stranded DNA-binding protein 2; SOSB2_HUMAN; SOSS B2; SOSS complex subunit B2; SOSS-B2; SSB2;

免疫原

免疫原:

A synthesized peptide derived from human OBFC2A, corresponding to a region within the internal amino acids.

Uniprot:
遺伝子(ID):
タンパク質配列:
MNRVNDPLIFIRDIKPGLKNLNVVFIVLEIGRVTKTKDGHEVRSCKVADKTGSITISVWDEIGGLIQPGDIIRLTRGYASMWKGCLTLYTGRGGELQKIGEFCMVYSEVPNFSEPNPDYRGQQNKGAQSEQKNNSMNSNMGTGTFGPVGNGVHTGPESREHQFSHAGRSNGRGLINPQLQGTASNQTVMTTISNGRDPRRAFKR

種類予測

種類予測:

Score>80(red) has high confidence and is suggested to be used for WB detection. *The prediction model is mainly based on the alignment of immunogen sequences, the results are for reference only, not as the basis of quality assurance.

Species
Results
Score
Rabbit
100
Pig
92
Horse
92
Dog
92
Bovine
86
Sheep
86
Chicken
67
Zebrafish
63
Xenopus
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

研究背景

機能:

Component of the SOSS complex, a multiprotein complex that functions downstream of the MRN complex to promote DNA repair and G2/M checkpoint. In the SOSS complex, acts as a sensor of single-stranded DNA that binds to single-stranded DNA, in particular to polypyrimidines. The SOSS complex associates with DNA lesions and influences diverse endpoints in the cellular DNA damage response including cell-cycle checkpoint activation, recombinational repair and maintenance of genomic stability. Required for efficient homologous recombination-dependent repair of double-strand breaks (DSBs) and ATM-dependent signaling pathways.

細胞の位置付け:

Nucleus.
Note: Localizes to nuclear foci following DNA damage.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
タンパク質ファミリー:

Belongs to the SOSS-B family. SOSS-B2 subfamily.

参考文献

1). The inhibition of ZC3H13 attenuates G2/M arrest and apoptosis by alleviating NABP1 m6A modification in cisplatin-induced acute kidney injury. Cellular and molecular life sciences : CMLS, 2025 (PubMed: 39985591) [IF=6.2]

Application: WB    Species: Mouse    Sample:

Fig. 5 NABP1 is a direct target of ZC3H13. (A) Venn diagrams show 1347 upregulated m6A modification mRNAs from GSE165100, 2223 upregulated genes from GSE153625, and 2745 upregulated genes from GSE142137; and the expressions of the 3 genes selected through the intersection of datasets. (B) Representative images of NABP1 IHC staining in kidney biopsies from AKI patients. (C) Western blotting analysis of NABP1 in AKI mice. (D-E) qPCR (D) and Western blotting (E) showed the induction of NABP1 by 10 µmol/L cisplatin for indicated hours in HK2 cells (n = 3). (F) Alterations in NABP1 m6A modifications in HK2 cells with or without cisplatin as determined by MeRIP-qPCR (n = 3). (G) The structures of the luciferase reporters. (H) The relative luciferase activity of WT group, CDS-mutant group, and 3’UTR-mutant group in the presence of cisplatin (n = 3). (I-K) NABP1 expression in HK2 cells exposed to cisplatin with ZC3H13 knockdown, as measured by qPCR (I; n = 3), Western blotting (J), and immunofluorescent staining (K). (L) Alterations in NABP1 m6A modification in HK2 cells with or without ZC3H13 knockdown as determined by MeRIP-qPCR (n = 3). (M) Alterations in NABP1 m6A modification in HK2 cells with or without ZC3H13 overexpression as determined by MeRIP-qPCR (n = 3). (N) Western blotting analysis of NABP1 in AKI mice with ZC3H13 knockdown. Data are showed as means ± SD. *P 

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