CLDN18 Antibody - #DF9392

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产品: CLDN18 抗体
货号: DF9392
描述: Rabbit polyclonal antibody to CLDN18
应用: WB IHC
文献验证: WB
反应: Human, Mouse, Rat, Monkey
预测: Pig, Bovine, Horse, Sheep, Rabbit
蛋白号: P56856
RRID: AB_2842588

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

货期: 当天发货

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产品描述

来源:
Rabbit
应用:
WB 1:1000-3000, IHC 1:50-1:200
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*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, Monkey
克隆:
Polyclonal
特异性:
CLDN18 Antibody detects endogenous levels of total CLDN18.
RRID:
AB_2842588
引用格式: Affinity Biosciences Cat# DF9392, RRID:AB_2842588.
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

Claudin 18; Claudin-18; CLD18_HUMAN; CLDN18; SFTA5; SFTPJ;

抗原和靶标

免疫原:

A synthesized peptide derived from human CLDN18, corresponding to a region within C-terminal amino acids.

基因/基因ID:
CLDN18(51208)

研究领域

· Cellular Processes > Cellular community - eukaryotes > Tight junction.   (View pathway)

· Environmental Information Processing > Signaling molecules and interaction > Cell adhesion molecules (CAMs).   (View pathway)

· Human Diseases > Infectious diseases: Viral > Hepatitis C.

· Organismal Systems > Immune system > Leukocyte transendothelial migration.   (View pathway)

文献引用

1). Early Radiation-Induced Changes in Lung Tissue and Intercellular Junctions: Implications for Tissue Repair and Fibrosis. Pathophysiology : the official journal of the International Society for Pathophysiology, 2024 (PubMed: 39449521) [IF=2.7]

Application: WB    Species: Rat    Sample:

Figure 4. E-cadherin, claudin-1, -3, -4, -5 -8, -12, -18, occludin, and tricellulin in rat lungs 72 h after IR at doses of 0, 2, and 10 Gy. (a) Representative blots. Full images of the Western blot are in the Supplementary Material (Figures S2–S12). (b,c) Western blot analysis of the intercellular junction proteins levels. The intensity of bends was normalized to the intensity of β-actin bends in the corresponding samples. One-way ANOVA followed by Tukey’s multiple comparisons test,

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