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MSR1 / CD204 Antikörper ( FITC )

Sino Biological Inc. liefert MSR1 / CD204 Antikörper ( FITC ) mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.

Weitere Informationen über MSR1 / CD204 Antikörper ( FITC ) lesen Sie bitte: http://www.sinobiological.com/MSR1-CD204-Antibody-g-10069.html

Produkt-Information von MSR1 / CD204 Antikörper

Immunogen

Recombinant Mouse MSR1 / CD204 protein (Catalog#50129-M07H)

Reagents FITC-conjugated rabbit monoclonal antibody

Clone ID

004

Ig Type

Rabbit IgG

Concentration

5 μl/Test, 0.2 mg/ml

Formulation Aqueous solution containing 0.5% BSA and 0.1% sodium azide
Preparation

This antibody was obtained from a rabbit immunized with purified, recombinant Mouse MSR1 / CD204 (rM MSR1 / CD204; Catalog#50129-M07H; AAH03814.1; Trp 83-Val 354) and conjugated with FITC under optimum conditions, the unreacted FITC was removed.

Usage Guide von MSR1 / CD204 Antikörper

Specificity

Mouse MSR1 / CD204

Flow Cytometry
MSR1 / CD204 Flow Cytometry

Profile of anti-MSR1 (CD204) reactivity on Raw264.7 cells analyzed by flow cytometry. Cells should be Fc-blocked by treatment with Mouse BD Fc Block™ purified anti-CD16/CD32 mAb 2.4G2 (Cat. No. 553141) prior to staining, washed, then stained with FITC Rabbit anti-MSR1 (CD204).

Flow cytometry was performed on a BD FACSCalibur flow cytometry system

Please refer to www.sinobiological.com/Flow-Cytometry-FACS-Protocols-a-750.html for technical protocols.

Storage This antibody is stable for 12 months from date of receipt when stored at 2℃-8℃. Protected from prolonged exposure to light. Do not freeze !
Sodium azide is toxic to cells and should be disposed of properly. Flush with large volumes of water during disposal.

Verwandte Produkte & Themen von MSR1 / CD204 Antikörper

Related Areas:

Immunology>>Innate Immunity>>Monocyte/Macrophage>>Scavenger Receptor>>MSR1/CD204

Immunology>>Cluster of Differentiation>>Monocyte/Macrophage CD Antigen>>Macrophage Markers>>MSR1/CD204

Proteins:
Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
MSR1/CD204/SCARA1 Human MSR1/CD204 Protein, Recombinant 10427-H07H
MSR1/CD204/SCARA1 Mouse MSR1/CD204 Protein, Recombinant 50129-M07H
MSR1/CD204/SCARA1 Rat MSR1 / SCARA1 Protein, Recombinant 80363-R01H
Antibodies:
Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Human
MSR1/CD204/SCARA1
WB, ELISA MSR1/CD204 Antibody, Mouse MAb 10427-MM02
Human
MSR1/CD204/SCARA1
WB, ELISA MSR1/CD204 Antibody, Rabbit MAb 10427-R005
Mouse
MSR1/CD204/SCARA1
WB, ELISA MSR1 / CD204 Antibody 50129-RP01
Mouse
MSR1/CD204/SCARA1
WB, ELISA MSR1 / CD204 Antibody (Antigen Affinity Purified) 50129-RP02
Human
MSR1/CD204/SCARA1
FCM MSR1 / CD204 Antibody ( FITC ) 50129-R004-F

MSR1 / CD204 Antibody Background

Macrophage scavenger receptor types I and II, also known as Macrophage acetylated LDL receptor I and II, Scavenger receptor class A member 1, CD204, MSR1 and SCARA1, is a single-pass type II membrane protein which contains onecollagen-like domain and oneSRCR domain. Macrophages are distributed in all peripheral tissues and play a critical role in the first line of the innate immune defenses against bacterial infection by phagocytosis of bacterial pathogens through the macrophage scavenger receptor 1 (MSR1). MSR1 / SCARA1 is one of the membrane glycoproteins implicated in the pathologic deposition of cholesterol in arterial walls during atherogenesis. Two types of receptor subunits exist. These receptors mediate the endocytosis of a diverse group of macromolecules, including modified low density lipoproteins (LDL). MSR1 / SCARA1 is also involved in chronic inflammation which is a risk factor for prostate cancer. MSR1 1 gene was identified as a candidate susceptibility gene for hereditary prostate cancer and as a risk factor for sporadic prostate cancer.

References

  1. Wang,L.et al., 2003, Nat Genet. 35 (2): 128-9.
  2. Chen,Y.C. et al., 2008, Cancer Epidemiol Biomarkers Prev17 (4): 1001-3.
  3. Shirato,K. et al., 2009,Pflugers Arch459 (1): 93-103.
  4. Sun,J.et al., 2006, Prostate. 66 (7): 728-37.

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