产品: Collagen Type VI 抗体
货号: DF12191
描述: Rabbit polyclonal antibody to Collagen Type VI
应用: WB IHC
文献验证: WB
反应: Human, Mouse, Rat
预测: Bovine, Sheep, Dog, Chicken
蛋白号: P12109
RRID: AB_2844996

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 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
*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
克隆:
Polyclonal
特异性:
Collagen Type VI Antibody detects endogenous levels of total Collagen Type VI.
RRID:
AB_2844996
引用格式: Affinity Biosciences Cat# DF12191, RRID:AB_2844996.
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

Alpha 1 (VI) chain (61 AA); CO6A1_HUMAN; COL6A1; Collagen alpha-1(VI) chain; Collagen VI, alpha 1 polypeptide; Collagen, intimal short chain collagen; Collagen, type VI, alpha 1; OPLL; OTTHUMP00000115501;

抗原和靶标

免疫原:

A synthesized peptide derived from human Collagen Type VI, 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). circ0066187 promotes pulmonary fibrogenesis through targeting STAT3-mediated metabolism signal pathway. Cellular and molecular life sciences : CMLS, 2025 (PubMed: 39969586) [IF=6.2]

Application: WB    Species: Mouse    Sample:

Fig. 9 Integrative analysis of proteomics and metabolomics. A Venn diagram showed three pathways co-enriched in proteomics and metabolomics, including Protein digestion and absorption, PI3K-Akt signaling pathway, and FoxO signaling pathway. B Interaction network diagram of differential proteins and metabolites among the three pathways. C Western blot verified that DPP4, CCND1, CDK2, and FGF2 were up-regulated and COL6A1 and SOD2 were down-regulated in the TGF-β1-treated MRC-5 cells and BLM-induced mice. D l-Glutamine, l-proline, and AMP increased, and l-arginine, l-phenylalanine, l-lysine, and l-tryptophan decreased in the TGF-β1-treated MRC-5 cells and BLM-induced mice. E Western blot demonstrated that circ0066187 knockdown decreased DPP4, CCND1, CDK2, and FGF2 expression and increased COL6A1 and SOD2 expression compared with those in TGF-β1-treated group. Circ0066187 overexpression enhanced DPP4, CCND1, CDK2, and FGF2 expression, and decreased COL6A1 and SOD2 expression. F miR-29b-2-5p mimic enhanced COL6A1 and SOD2 expression and inhibited DPP4, CCND1, CDK2, and FGF2 expression. miR-29b-2-5p inhibitor enhanced DPP4, CCND1, CDK2, and FGF2 expression and inhibited COL6A1 and SOD2 expression. G Rescue experiment of Western blot demonstrated that the miR-29b-2-5p inhibitor reversed the downward trend of DPP4, CCND1, CDK2, and FGF2 and the upward trend of COL6A1 and SOD2 caused by si-circ0066187. miR-29b-2-5p mimic reversed the upward trend of DPP4, CCND1, CDK2, and FGF2 and the downward trend of COL6A1 and SOD2 caused by circ0066187 overexpression. H Western blot showed that si-STAT3 decreased DPP4, CCND1, CDK2, and FGF2 expression, and increased COL6A1 and SOD2 expression. Overexpressed STAT3 enhanced DPP4, CCND1, CDK2, and FGF2 expression and inhibited COL6A1 and SOD2 expression. I Rescue experiment showed that STAT3 overexpression reversed the downward trend of DPP4, CCND1, CDK2, and FGF2 and the upward trend of COL6A1 and SOD2 caused by si-circ0066187. si-STAT3 reversed the upward trend of DPP4, CCND1, CDK2, and FGF2 and the downward trend of COL6A1 and SOD2 caused by circ0066187 overexpression. NC represents negative control, BP represents blank plasmid, and RP represents the recombinant plasmid of overexpressed circ0066187. OE-STAT3 represents overexpressed STAT3. Each bar represents the mean ± SD; n = 6; *p 

2). FBN1 knockout promotes cervical artery dissection by inducing N-glycosylation alternation of extracellular matrix proteins in rat VSMCs. Cellular signalling, 2023 (PubMed: 37532137) [IF=4.4]

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