biological source
rabbit
conjugate
unconjugated
antibody form
purified antibody
antibody product type
primary antibodies
clone
polyclonal
species reactivity
mouse
manufacturer/tradename
Chemicon®
technique(s)
ELISA: suitable, immunofluorescence: suitable, immunohistochemistry: suitable (paraffin)
suitability
not suitable for Western blot
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Quality Level
General description
139 kDa (unprocessed precursor)
Collagen Type IV extracted and purified from mouse tumor tissues. Antibody shows less than 0.1% reactivity with human Collagen types IV, V and mouse Collagen Types I, II, III and mouse Fibronectin and Laminin.
Collagen is the main protein of connective tissue in animals and the most abundant protein in mammals, making up about 25% of the total protein content. It is one of the long, fibrous structural proteins whose functions are quite different from those of globular proteins such as enzymes; tough bundles of collagen called collagen fibers are a major component of the extracellular matrix that supports most tissues and gives cells structure from the outside, but collagen is also found inside certain cells. Collagen has great tensile strength, and is the main component of fascia, cartilage, ligaments, tendons, bone and teeth. Along with soft keratin, it is responsible for skin strength and elasticity, and its degradation leads to wrinkles that accompany aging. It strengthens blood vessels and plays a role in tissue development. It is present in the cornea and lens of the eye in crystalline form. Collagen occurs in many places throughout the body. There are 12 types of collagen described in literature. Collagen Type 1: This is the most abundant collagen of the human body. It is present in scar tissue, the end product when tissue heals by repair. It is found in tendons, the endomysium of myofibrils and the organic part of bone. Collagen Type 4: It is present in basal lamina and the eye lens. Also serves as part of the filtration system in capillaries and the glomeruli of nephron in the kidney.
Immunogen
Collagen Type IV extracted and purified from mouse tumor tissues.
Application
ELISA:
A previous lot of this antibody was used in ELISA at >1:200 (OD >500).
Immunofluorescence:
A previous lot of this antibody was used in immunofluorescence.
Immunohistochemistry:
1:80 dilution for immunofluorescent staining of fresh frozen mouse skin and liver tissues. Acetone or methyl-carnoy fixed paraffin-embedded tissue (mouse skin and liver) is also reactive.
Not recommended for Western blots.
Optimal working dilutions must be determined by end user.
A previous lot of this antibody was used in ELISA at >1:200 (OD >500).
Immunofluorescence:
A previous lot of this antibody was used in immunofluorescence.
Immunohistochemistry:
1:80 dilution for immunofluorescent staining of fresh frozen mouse skin and liver tissues. Acetone or methyl-carnoy fixed paraffin-embedded tissue (mouse skin and liver) is also reactive.
Not recommended for Western blots.
Optimal working dilutions must be determined by end user.
Research Category
Cell Structure
Cell Structure
Research Sub Category
ECM Proteins
ECM Proteins
This Anti-Collagen Antibody, Type IV is validated for use in ELISA, IF, IH(P) for the detection of Collagen.
Biochem/physiol Actions
Antibody shows less than 0.1% reactivity with human Collagen types IV, V and mouse Collagen Types I, II, III, mouse Fibronectin, and mouse laminin.
Mouse Collagen, Type IV: 100 (%’s at a 1:5000 RIA dilution) Mouse Collagen, Types I, II, III: <0.1 Human Collagen, Types IV, V: <0.1 Mouse Fibronectin: <0.1 Mouse Laminin: <0.1 Reactivity with other species has not been determined.
Physical form
Format: Purified
Protein G Purified
The purified antibody is supplied in a buffer containing a mixture of 0.1M Citrate, 0.1M potassium phosphate, at a pH of 7.2-7.4 and 10µl/ml of antibiotics and antimycotics.
Preparation Note
Stable for 1 year at -20ºC from date of receipt.
Analysis Note
Control
Positive Control: Kidney, muscle, tendon spleen tissue, mouse liver. Negative Control: Neurons/glia.
Positive Control: Kidney, muscle, tendon spleen tissue, mouse liver. Negative Control: Neurons/glia.
Other Notes
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
Replaces: AB756
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
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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저장 등급
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Long-term retinal PEDF overexpression prevents neovascularization in a murine adult model of retinopathy.
Haurigot, V; Villacampa, P; Ribera, A; Bosch, A; Ramos, D; Ruberte, J; Bosch, F
Testing null
Magdalena Leiva et al.
Nature communications, 7, 10222-10222 (2016-01-09)
The life-long maintenance of haematopoietic stem and progenitor cells (HSPCs) critically relies on environmental signals produced by cells that constitute the haematopoietic niche. Here we report a cell-intrinsic mechanism whereby haematopoietic cells limit proliferation within the bone marrow, and show
Fabienna Arends et al.
PloS one, 10(2), e0118090-e0118090 (2015-02-18)
The migration of cells within a three-dimensional extracellular matrix (ECM) depends sensitively on the biochemical and biophysical properties of the matrix. An example for a biological ECM is given by reconstituted basal lamina gels purified from the Engelbreth-Holm-Swarm sarcoma of
Ann S Grosse et al.
Development (Cambridge, England), 138(20), 4423-4432 (2011-09-02)
The cellular mechanisms that drive growth and remodeling of the early intestinal epithelium are poorly understood. Current dogma suggests that the murine fetal intestinal epithelium is stratified, that villi are formed by an epithelial remodeling process involving the de novo
Mitsunobu R Kano et al.
Journal of cell science, 118(Pt 16), 3759-3768 (2005-08-18)
Combined stimulation with VEGF-A, FGF-2, or PDGF-BB has emerged as a potent strategy for therapeutic angiogenesis, although the mechanisms underlying the synergism of these factors are not well understood. In the present study, we investigated the mechanism of synergism between
국제 무역 품목 번호
| SKU | GTIN |
|---|---|
| AB756P | 04053252272660 |
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