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Human ABCD1 ELISA Kit

  • Product Information
  • Description
Catalog: C-EL-1934T
Product Type: Test kit
Size: 96 tests
Principle: Sandwich ELISA
Species: Human
Detection range: 31.25-2000 pg/mL
Sensitivity: 6.0 pg/mL
Sample type: Serum, Plasma, cell lysates
Test type: Quantitative
Analysis mode: ELISA
Storage: All the reagents are stored at 2-8℃. Refer to the protocol for further storage instructions.
Synonyms:: ABC42, ABCD1, Adrenoleukodystrophy protein, ALD, ALDP, AMN
Application: Vascular endothelial growth factor (VEGF), is a signal protein produced by cells that stimulates vasculogenesis and angiogenesis. It is part of the system that restores the oxygen supply to tissues when blood circulation is inadequate such as in hypoxic conditions. Serum concentration of VEGF is high in bronchial asthma and diabetes mellitus. The activities of VEGF are not limited to the vascular system; VEGF plays a role in normal physiological functions such as bone formation, hematopoiesis, wound healing, and development. Disruption of this gene in mice resulted in abnormal embryonic blood vessel formation. VEGF is upregulated in many known tumors and its expression is correlated with tumor stage and progression.

This test kit is a solid phase sandwich Enzyme Linked-Immuno-Sorbent Assay (Sandwich ELISA). The ABCD1 ELISA kit is to be used to detect and quantify protein levels of endogenous ABCD1. The assay recognizes human ABCD1. An antibody specific for ABCD1 has been pre-coated onto the microwells. The ABCD1 protein in samples is captured by the coated antibody after incubation. Following extensive washing, another antibody specific for ABCD1 is added to detect the captured ABCD1 protein. For signal development, horseradish peroxidase (HRP)-conjugated antibody is added, followed by Tetramethyl-benzidine (TMB) reagent. Solution containing sulfuric acid is used to stop color development and the color intensity which is proportional to the quantity of bound protein is measurable at 450nm with the correction wavelength set at 630 nm.

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