Goat Anti-Mouse IgG (H+L) FITC -conjugated - #S0007
| Product: | Goat Anti-Mouse IgG (H+L) FITC -conjugated |
| Catalog: | S0007 |
| Source: | Goat |
| Application: | WB IF/ICC FACS |
| Reactivity: | Mouse |
| RRID: | AB_2843438 |
Product Info
Source:
Goat
Application:
WB 1:100 – 1:500, IF/ICC 1:100 – 1:500
*The optimal dilutions should be determined by the end user.
*The optimal dilutions should be determined by the end user.
Reactivity:
Mouse
Clonality:
Polyclonal
RRID:
AB_2843438
Cite Format: Affinity Biosciences Cat# S0007, RRID:AB_2843438.
Cite Format: Affinity Biosciences Cat# S0007, RRID:AB_2843438.
Conjugate:
FITC. Ex:495nm/Em:520nm
Purification:
affinity purification.
Concentration:
1mg/ml
Storage:
0.01M Sodium phosphate, 0.25M NaCl, 50% glycerol, pH7.6.Store at -20℃，avoid repeated thawing and freezing.
Immunogens
Immunogen:
The antiserum was developed in goat using the MOUSE IgG as the immunogen.
References
1). Jiang Y et al. Hedgehog pathway inhibition causes primary follicle atresia and decreases female germline stem cell proliferation capacity or stemness. Stem Cell Research & Therapy 2019 Jul 5;10(1):198 (PubMed: 31277696)
[IF=7.5]
2). Zhang et al. Chemerin-Induced Down-Regulation of Placenta-Derived Exosomal miR-140-3p and miR-574-3p Promotes Umbilical Vein Endothelial Cells Proliferation, Migration, and Tube Formation in Gestational Diabetes Mellitus. Cells 2022 Nov 1;11(21):3457. (PubMed: 36359855)
[IF=6.0]
3). Zhou H et al. Orthosilicic Acid Accelerates Bone Formation in Human Osteoblast-Like Cells Through the PI3K-Akt-mTOR Pathway. BIOLOGICAL TRACE ELEMENT RESEARCH 2018 Nov 12 (PubMed: 30421162)
[IF=3.9]
4). Liu Q et al. Leptin promotes fatty acid oxidation and OXPHOS via the c-Myc/PGC-1 pathway in cancer cells. ACTA BIOCHIMICA ET BIOPHYSICA SINICA 2019 Jul 10;51(7):707-714 (PubMed: 31187140)
[IF=3.7]
5). Dong S et al. Carbenoxolone has the potential to ameliorate acute incision pain in rats. Molecular Medicine Reports 2021 Jul;24(1):520. (PubMed: 34013377)
[IF=3.4]
6). Gulimiran Alitongbieke et al. Effect of β-chitosan on the binding interaction between SARS-CoV-2 S-RBD and ACE2. bioRxiv
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