产品: OBFC2A 抗体
货号: DF12433
描述: Rabbit polyclonal antibody to OBFC2A
应用: WB IHC IF/ICC
文献验证: WB
反应: Human
预测: Pig, Bovine, Horse, Sheep, Rabbit, Dog
蛋白号: Q96AH0
RRID: AB_2845238

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   规格 价格 库存
 50ul RMB¥ 1250 现货
 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

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产品描述

来源:
Rabbit
应用:
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.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human
克隆:
Polyclonal
特异性:
OBFC2A Antibody detects endogenous levels of total OBFC2A.
RRID:
AB_2845238
引用格式: Affinity Biosciences Cat# DF12433, RRID:AB_2845238.
偶联:
Unconjugated.
纯化:
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.
别名:

展开/折叠

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;

抗原和靶标

免疫原:

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

基因/基因ID:

文献引用

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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