产品: Collagen VI alpha 2 抗体
货号: DF3552
描述: Rabbit polyclonal antibody to Collagen VI alpha 2
应用: WB IHC IF/ICC
文献验证: WB, IF/ICC
反应: Human, Rat
预测: Pig, Bovine, Horse, Sheep, Rabbit, Dog
蛋白号: P12110
RRID: AB_2835925

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产品描述

来源:
Rabbit
应用:
WB 1:500-1:1000, 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, Rat
克隆:
Polyclonal
特异性:
Collagen VI alpha 2 Antibody detects endogenous levels of total Collagen VI alpha 2.
RRID:
AB_2835925
引用格式: Affinity Biosciences Cat# DF3552, RRID:AB_2835925.
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

CO6A2_HUMAN; COL6A2; Collagen alpha 2(VI) chain; Collagen alpha-2(VI) chain; collagen type VI alpha 2; Collagen VI alpha 2 polypeptide; human mRNA for collagen VI alpha 2 C terminal globular domain; PP3610;

抗原和靶标

免疫原:

A synthesized peptide derived from human Collagen VI alpha 2, corresponding to a region within the internal amino acids.

基因/基因ID:

研究领域

· Cellular Processes > Cellular community - eukaryotes > Focal adhesion.   (View pathway)

· Environmental Information Processing > Signal transduction > PI3K-Akt signaling pathway.   (View pathway)

· Environmental Information Processing > Signaling molecules and interaction > ECM-receptor interaction.   (View pathway)

· Human Diseases > Infectious diseases: Viral > Human papillomavirus infection.

· Organismal Systems > Digestive system > Protein digestion and absorption.

文献引用

1). Identification of prothymosin alpha (PTMA) as a biomarker for esophageal squamous cell carcinoma (ESCC) by label-free quantitative proteomics and Quantitative Dot Blot (QDB). Clinical Proteomics, 2019 (PubMed: 30988666) [IF=2.8]

Application: WB    Species: human    Sample: ESCC tissues

Fig. 5|The diferentially expressed proteins were validated by Western Blot. Compared with adjacent normal tissues, the protein expression of PTMA, PAK2, PPP1CA, HMGB2 were up-regulated (a, b), and the protein expression of Caveolin, Integrin beta-1, Collagen alpha-2(VI), Leiomodin-1, Vinculin were down-regulated in ESCC tissues from four pairs of samples (c, d). Representative immunoblot images (a, c) and histograms (mean ± SD; b, d).The experiments were repeated at least three times, N represented normal tissues and T represented tumor tissues

2). Effects of phytoestrogens combined with cold stress on sperm parameters and testicular proteomics in rats. Open life sciences, 2023 (PubMed: 36742450) [IF=1.7]

Application: WB    Species: Rat    Sample:

Figure3 ITGA6 was downregulated, Col6α1 and Col6α2 were upregulated in the testis of the model group exposed to an estrogen-enriched diet and cold for 24 weeks. (a) Immunofluorescence staining for ITGA6 (red, 200×), Col6α1 (green, 100×), Col6α2 (red, 100×); nuclei were stained with DAPI (blue). (b, c, and d) Representative western blot results for ITGA6, Col6α1, Col6α2. (e, f, and g) Relative expression of ITGA6, Col6α1, Col6α2 compared with GAPDH. Protein lysates were obtained from the testis of either model (M) or control rat group (N). Protein expression of ITGA6, Col6α1, and Col6α2 was evaluated by western blotting using specific antibodies for the target proteins, and the signal was then quantified using Image J. (h, i, and j) qRT-PCR of ITGA6, Col6α1, and Col6α2 in the testis of rats in the two groups. Values are expressed as the mean ± SD. Statistical significance is indicated as * P < 0.05, ** P < 0.01, and *** P < 0.001 compared to the control group.

Application: IF/ICC    Species: Rat    Sample:

Figure3 ITGA6 was downregulated, Col6α1 and Col6α2 were upregulated in the testis of the model group exposed to an estrogen-enriched diet and cold for 24 weeks. (a) Immunofluorescence staining for ITGA6 (red, 200×), Col6α1 (green, 100×), Col6α2 (red, 100×); nuclei were stained with DAPI (blue). (b, c, and d) Representative western blot results for ITGA6, Col6α1, Col6α2. (e, f, and g) Relative expression of ITGA6, Col6α1, Col6α2 compared with GAPDH. Protein lysates were obtained from the testis of either model (M) or control rat group (N). Protein expression of ITGA6, Col6α1, and Col6α2 was evaluated by western blotting using specific antibodies for the target proteins, and the signal was then quantified using Image J. (h, i, and j) qRT-PCR of ITGA6, Col6α1, and Col6α2 in the testis of rats in the two groups. Values are expressed as the mean ± SD. Statistical significance is indicated as * P < 0.05, ** P < 0.01, and *** P < 0.001 compared to the control group.

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