产品: UNC5B 抗体
货号: DF13685
描述: Rabbit polyclonal antibody to UNC5B
应用: WB IF/ICC
文献验证: WB, IF/ICC
反应: Human, Mouse, Rat
预测: Pig, Bovine, Horse, Sheep, Rabbit, Dog, Chicken, Xenopus
蛋白号: Q8IZJ1
RRID: AB_2846704

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 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

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产品描述

来源:
Rabbit
应用:
IF/ICC 1:100-1:500, WB 1:500-1:2000
*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, Mouse, Rat
克隆:
Polyclonal
特异性:
UNC5B Antibody detects endogenous levels of total UNC5B.
RRID:
AB_2846704
引用格式: Affinity Biosciences Cat# DF13685, RRID:AB_2846704.
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

6330415E02Rik; A630020F16; D10Bwg0792e; Netrin receptor UNC5B; Netrin receptor UNC5B Precursor; p53 regulated receptor for death and life; p53 regulated receptor for death and life protein 1; p53-regulated receptor for death and life protein 1; p53RDL1; Protein unc-5 homolog 2; Protein unc-5 homolog B; Protein XUNC 5; Transmembrane receptor Unc5H2; Unc 5 homolog 2; Unc 5 homolog B; Unc 5 netrin receptor B; UNC 5B; Unc5 (C.elegans homolog) b; Unc5b; UNC5B_HUMAN; UNC5H2;

抗原和靶标

免疫原:

A synthesized peptide derived from human UNC5B, corresponding to a region within the internal amino acids.

基因/基因ID:

研究领域

· Organismal Systems > Development > Axon guidance.   (View pathway)

文献引用

1). PTBP1 knockdown promotes neural differentiation of glioblastoma cells through UNC5B receptor. Theranostics, 2022 (PubMed: 35664063) [IF=12.4]

Application: WB    Species: Human    Sample: U251 cells

Figure 6 UNC5B receptor is a key in reprogramming generated by PTBP1 knockdown. (A-C) KI67 and TUJ1 staining revealed the reprogramming efficiency of particular lentiviruses-infected U251 cells (9 random fields from triplicate samples were captured for quantification; TUJ1+ (%) = TUJ1+ M-cherry+/M-cherry+; KI67+ (%) = KI67+ M-cherry+/M-cherry+; M-cherry+ cells = 128-566 for each condition). (D, E) Western blot analysis of UNC5B protein in U251 cells infected with sh-Luci and sh-PTBP1 for 3 and 7 days. (n = 3). (F, G) The change of UNC5B protein expression under the state of PTBP1 overexpression. (n = 3). GAPDH was used as an internal reference protein. The data are presented as mean ± SD. ***P < 0.001, ###P < 0.001 vs. sh-PTBP1, sh-Luci, sh-Luci-3d or control vector group. Dpi (d): days post infection; ND: not detected; NS (ns): no significance; OE: overexpression. Scale: 100 µm.

2). Activation of vascular endothelial cells by synovial fibrosis promotes Netrin-1-induced sensory nerve sprouting and exacerbates pain sensitivity. Journal of cellular and molecular medicine, 2023 (PubMed: 37702437) [IF=5.3]

Application: WB    Species: Rat    Sample: DRG tissues

FIGURE 2 KOA synovial fibrosis initiates Netrin-1 induction of sensory nerve germination. (A) Each group of DRG tissues was immunofluorescently stained using βIII-Tubulin + DCC + DAPI at 200× scale bar = 50 μm to observe the expression of DRG markers and DCC, an indicator of nerve sprouting. (B) Each group of DRG tissues was immunofluorescently stained using βIII-Tubulin + UNC5 + DAPI, 200× scale bar = 50 μm, to observe the expression of DRG markers and UNC5, an indicator of nerve sprouting. (C–E) WB and PCR were performed to detect the protein and gene expression of GAP43, DCC and UNC5, the neural sprouting-related indicators in DRG tissues of each group of rats. (*p 

Application: IF/ICC    Species: Rat    Sample: DRG tissues

FIGURE 2 KOA synovial fibrosis initiates Netrin-1 induction of sensory nerve germination. (A) Each group of DRG tissues was immunofluorescently stained using βIII-Tubulin + DCC + DAPI at 200× scale bar = 50 μm to observe the expression of DRG markers and DCC, an indicator of nerve sprouting. (B) Each group of DRG tissues was immunofluorescently stained using βIII-Tubulin + UNC5 + DAPI, 200× scale bar = 50 μm, to observe the expression of DRG markers and UNC5, an indicator of nerve sprouting. (C–E) WB and PCR were performed to detect the protein and gene expression of GAP43, DCC and UNC5, the neural sprouting-related indicators in DRG tissues of each group of rats. (*p 

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