生物来源
mouse
质量水平
抗体形式
purified immunoglobulin
抗体产品类型
primary antibodies
克隆
PCIDG10, monoclonal
种属反应性
mouse, human, rat, guinea pig
种属反应性(根据同源性预测)
bovine (based on 100% sequence homology)
技术
ELISA: suitable
flow cytometry: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable (paraffin)
同位素/亚型
IgG1κ
NCBI登记号
UniProt登记号
运输
dry ice
靶向翻译后修饰
unmodified
基因信息
human ... COL1A1(1277)
相关类别
一般描述
Collagen alpha-1(I) chain (UniProt P02452; also known as Alpha-1 type I collagen) is encoded by the COL1A1 gene (Gene ID 1277) in human. Collagen is the major component of the extracellular matrix (ECM) and forms the fibrils of tendons, ligaments, and bones. Type I collagen consists of two alpha I chains and one alpha 2 chain. Alpha-1 type I collagen is initially produced as a 1464-amino acid prepro-form with a signal peptide sequence (a.a. 1-22) and two propeptide sequences (a.a. 23-161 and a.a. 1219 –1464), the removal of which yields the mature alpha-1(I) chain. The mature alpha-1(I) chain is composed mostly of a large triple-helical region (a.a. 179-1192) sandwiched between two nonhelical segments known as the N-terminal telopeptide (a.a. 162-178; numbering based on the prepro-form) and the C-terminal telopeptide (a.a. 1193-1218; numbering based on the prepro-form). Collagen can be extracted from tissue via either enzymatic or non-enzymatic means. Collagen extracted using the proteolytic enzyme pepsin corresponds to the large triple-helical region, referred to as atelocollagen because both the N- and C-terminal telopeptides have been cleaved off by pepsin. On the other hand, collagen preparations obtained with non-enzymatic means (e.g. by acid extraction) have the intact telopeptides at both ends.
特异性
Labels carboxy-terminal pro-peptide of collagen type I. Does not stain mature collagen fibers in tissue, but rather is localized intracellularly in cells producing pro-collagen I.
免疫原
Epitope: C-terminal propeptide region
Human pro-collagen I.
应用
Immunohistochemistry Analysis: A 1:50 dilution from a representative lot detected Procollagen Type I in mouse skin, rat skin, and rat skeletal muscle tissue.
Immunocytochemistry Analysis: A representative lot detected type I procollagen immunoreactivity in human semitendinosus and gracilis tendon fibroblasts from patients undergoing reconstruction surgery after anterior cruciate ligament (ACL) rupture by fluorescent immunocytochemistry (Bayer, M.L., et al. (2012). Mech Ageing Dev. 133(5):246-254).
Flow Cytometry Analysis: A representative lot detected PICP+/CD45+ fibrocytes in lung cells from bleomycin-treated mice (Yeager, M.E., et al. (2012). Eur Respir J. 39(1):104-111).
Flow Cytometry Analysis: A representative lot detected higher numbers and percentages of circulating PICP+/CD45+ fibrocytes in peripheral blood samples from children/yound adults with pulmonary hypertension (PH) than in samples from healthy individuals (Reese, C., et al. (2014). Front Pharmacol. 5:141).
Immunohistochemistry Analysis: A representative lot detected cytoplasmic type I procollagen immunoreactivity in stromal cells from the lysed functionalis of frozen human menstrual endometria sections (Gaide Chevronnay, H.P., et al. (2009). Endocrinology. 150(11):5094-5105).
ELISA Analysis: A representative lot detected different age-dependency of procollagen type I C-terminal propeptide (PICP) immunoreactivity in the cruciate ligaments of osteoarthritis-/OA-prone Dunkin-Hartley (DH) guinea pigs and in age-matched Bristol strain 2 (BS2) control guinea pigs (Quasnichka, H.L., et al. (2005). Arthritis Rheum. 52(10):3100-3109).
Immunocytochemistry Analysis: A representative lot detected type I procollagen immunoreactivity in human semitendinosus and gracilis tendon fibroblasts from patients undergoing reconstruction surgery after anterior cruciate ligament (ACL) rupture by fluorescent immunocytochemistry (Bayer, M.L., et al. (2012). Mech Ageing Dev. 133(5):246-254).
Flow Cytometry Analysis: A representative lot detected PICP+/CD45+ fibrocytes in lung cells from bleomycin-treated mice (Yeager, M.E., et al. (2012). Eur Respir J. 39(1):104-111).
Flow Cytometry Analysis: A representative lot detected higher numbers and percentages of circulating PICP+/CD45+ fibrocytes in peripheral blood samples from children/yound adults with pulmonary hypertension (PH) than in samples from healthy individuals (Reese, C., et al. (2014). Front Pharmacol. 5:141).
Immunohistochemistry Analysis: A representative lot detected cytoplasmic type I procollagen immunoreactivity in stromal cells from the lysed functionalis of frozen human menstrual endometria sections (Gaide Chevronnay, H.P., et al. (2009). Endocrinology. 150(11):5094-5105).
ELISA Analysis: A representative lot detected different age-dependency of procollagen type I C-terminal propeptide (PICP) immunoreactivity in the cruciate ligaments of osteoarthritis-/OA-prone Dunkin-Hartley (DH) guinea pigs and in age-matched Bristol strain 2 (BS2) control guinea pigs (Quasnichka, H.L., et al. (2005). Arthritis Rheum. 52(10):3100-3109).
Research Category
Cell Structure
Cell Structure
Research Sub Category
Adhesion (CAMs)
Adhesion (CAMs)
This Anti-Procollagen Type I Antibody, CT, clone PCIDG10 (Ascites Free) is validated for use in Immunohistochemistry (Paraffin), Immunocytochemistry, Flow Cytometry and ELISA for the detection of Procollagen Type I.
质量
Evaluated by Immunohistochemistry in human bone tissue.
Immunohistochemistry Analysis: A 1:50 dilution of this antibody detected Procollagen Type I in human bone tissue.
Immunohistochemistry Analysis: A 1:50 dilution of this antibody detected Procollagen Type I in human bone tissue.
目标描述
140 kDa calculated
外形
Protein G Purified
Format: Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl without preservatives.
储存及稳定性
Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
其他说明
Concentration: Please refer to lot specific datasheet.
免责声明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Endocrinology, 150(11), 5094-5105 (2009-10-13)
Coupling of focal degradation and renewal of the functional layer of menstrual endometrium is a key event of the female reproductive biology. The precise mechanisms by which the various endometrial cell populations control extracellular matrix (ECM) degradation in the functionalis
The Journal of clinical investigation, 78(5), 1237-1244 (1986-11-01)
Excessive collagen deposition plays a critical role in the development of fibrosis, and early or active fibrosis may be more susceptible to therapeutic intervention than later stages of scarring. However, at present there is no simple method for assessing the
International heart journal, 64(4), 632-640 (2023-07-31)
Atrial fibrillation (AF) is the most common arrhythmia that is harmful to human health. This study aims to explore the relationship between myosin light chain 4 (MYL4) and AF recurrence after radiofrequency ablation (RFA). Patients with AF (n = 85)
Mechanisms of ageing and development, 133(5), 246-254 (2012-03-08)
The aging process of tendon tissue is associated with decreased collagen content and increased risk for injuries. An essential factor in tendon physiology is transforming growth factor-β1 (TGF-β1), which is presumed to be reduced systemically with advanced age. The aim
Arthritis and rheumatism, 52(10), 3100-3109 (2005-10-04)
The influence of the cruciate ligaments in spontaneous osteoarthritis (OA) is not understood, although ligament rupture is known to cause secondary OA. Additionally, femoral notch narrowing at the anterior cruciate ligament (ACL) insertion site is associated with disease severity, but
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