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Rabbit Polyclonal CollagenXIalpha Antibody

  • 中文名: Collagen XI alpha抗体
  • 别    名: Collagen alpha-1(XI) chain [Precursor]; COBA1;
货号: IPDX42185
Price: ¥1180
数量:
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验证与应用

应用及物种
WB 咨询技术 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 咨询技术 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesCollagen alpha-1(XI) chain [Precursor]; COBA1;
Entrez GeneID1301;
WB Predicted band size181kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman,Mouse
ImmunogenSynthesized peptide derived from internal of human Collagen XI alpha1.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于Collagen XI alpha抗体的3篇参考文献示例(内容基于模拟数据):

1. **文献名称**:*"Collagen XI α1 facilitates cartilage development by regulating fibril assembly"*

**作者**:Yoshioka, H. et al.

**摘要**:研究通过免疫组化和Western blot分析COL11A1在软骨中的表达,发现其通过调控II型胶原纤维的组装影响软骨分化,抗体特异性验证显示其在发育中起关键作用。

2. **文献名称**:*"Role of collagen XI in extracellular matrix structure: Insights from antibody-based disruption studies"*

**作者**:Birk, D.E. & Trelstad, R.L.

**摘要**:利用胶原XI alpha抗体阻断功能,证实COLXI在维持胶原纤维直径和基质完整性中不可或缺,敲低模型显示纤维结构异常。

3. **文献名称**:*"COL11A1 mutations and antibody localization in zebrafish skeletal dysplasia models"*

**作者**:Asharani, P.V. et al.

**摘要**:在斑马鱼模型中,抗体验证COL11A1突变导致颅面骨骼畸形,免疫荧光显示突变体软骨胶原分布紊乱,提示其在骨骼发育中的保守功能。

4. **文献名称**:*"Altered collagen XI expression in osteoarthritis: A comparative immunohistochemical study"*

**作者**:Sztrolovics, R. et al.

**摘要**:对比骨关节炎患者与正常关节软骨,发现COL11A1抗体标记强度显著升高,提示其与疾病进展中基质重塑相关。

(注:以上文献为示例,实际引用需根据具体研究检索PubMed等数据库。)

背景信息

Collagen XI alpha 1 (COL11A1) antibody is a tool used to study the α1 chain of type XI collagen, a minor fibrillar collagen critical for extracellular matrix (ECM) organization. Type XI collagen, composed of three α chains (α1. α2. α3), is closely associated with type II collagen in cartilage, vitreous humor, and other tissues, where it regulates fibril diameter and ECM stability. COL11A1 mutations are linked to skeletal dysplasias like Stickler syndrome, Marshall syndrome, and fibrochondrogenesis, characterized by craniofacial abnormalities, hearing loss, and joint issues. Additionally, COL11A1 overexpression is implicated in cancer progression, particularly in ovarian, gastric, and lung cancers, where it may promote epithelial-mesenchymal transition (EMT) and metastasis.

The COL11A1 antibody aids in detecting this protein in research applications such as immunohistochemistry, Western blotting, and immunofluorescence. It helps elucidate COL11A1's role in tissue development, disease mechanisms, and potential therapeutic targeting. Studies using this antibody have advanced understanding of how COL11A1 interacts with other collagens and growth factors to influence cell adhesion, tissue morphogenesis, and pathological processes. Its specificity and reliability make it valuable for both basic research and clinical investigations into connective tissue disorders and cancer biology.

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