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AdipoGen Life Sciences
anti-CTRP5 (human), pAb
1: Human CTRP5 (tGD) (His-tagged).
2: Human CTRP5 (His-tagged).
3: Human CTRP5 (GD) (His-tagged) (negative control).
4: Human CTRP6 (His-tagged) (negative control).
5: Human CTRP6 (GD) (His-tagged) (negative control).
6: Human CTRP7 (GD) (His-tagged) (negative control).
7: Human CTRP9 (GD) (His-tagged) (negative control).
8: Human CTRP10 (GD) (His-tagged) (negative control).
9: Mouse FTO (His-tagged) (negative control).
Product Details | |
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Synonyms | Complement C1q Tumor Necrosis Factor-related Protein 5; C1QTNF5 |
Product Type | Polyclonal Antibody |
Properties | |
Source/Host | Rabbit |
Immunogen/Antigen | Recombinant human CTRP5. |
Application |
ELISA: (direct and indirect: 1:2’000-1:5’000) Note: Tested on recombinant proteins and/or target-protein transfected cell lines in ELISA, Western Blot and/or FACS. |
Crossreactivity | Human |
Specificity |
Recognizes the N-terminal half of CTRP5 full-length protein. Detects bands of ~15kDa and ~26kDa by Western blot. |
Purity Detail | Protein A-affinity purified. |
Concentration | 1mg/ml |
Formulation | Liquid. 0.2μm-filtered solution in PBS, pH 7.4. Contains no preservatives. |
Isotype Negative Control | |
Shipping and Handling | |
Shipping | BLUE ICE |
Short Term Storage | +4°C |
Long Term Storage | -20°C |
Handling Advice |
After opening, prepare aliquots and store at -20°C. Avoid freeze/thaw cycles. |
Use/Stability | Stable for at least 6 months after receipt when stored at -20°C. |
Documents | |
MSDS | Download PDF |
Product Specification Sheet | |
Datasheet | Download PDF |
CTRP5 (C1qTNF-related protein 5; C1QTNF5) belongs to a highly conserved family of adiponectin paralogs. CTRP5 mediates activation of AMP-activated protein kinase (AMPK) in muscle and liver cells, thereby regulating glucose and lipid metabolism. Serum levels of CTRP5 are significantly higher in obese/diabetic animal models compared to normal controls. Furthermore, CTRP5 may be a putative biomarker for mitochondrial dysfunction. Defects in C1QTNF5 are a cause of late-onset retinal degeneration (LORD).