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Bovine Transcobalamin-2 (TCN2) ELISA Kit-Sandwich

Name: Bovine Transcobalamin-2 (TCN2) ELISA Kit-Sandwich
SKU: EK11F574
Rating: 5 (1 reviews)

Cat. No.EK11F574

Product TypeAnimal Immunoassay Kits

Size

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Product Overview

BioVenic Bovine Transcobalamin-2 (TCN2) ELISA Kit-Sandwich is designed for the quantitative determination of Bovine Transcobalamin-2 (TCN2) in serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids using a Sandwich ELISA method. For research use only.

Specifications

Assay Type ELISA-Sandwich

Specificity The assay kit is specific for Bovine TCN2.

Target Species Bovine

Species Reactivity Bovine

Reproducibility Intra-Assay: CV < 10%; Inter-Assay: CV < 10%

Assay Time Around 270 min

Sample Requirement Serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids.

Target Information

Transcobalamin-2 (TCN2), which is also known as holo-transcobalamin, is a protein involved in the transport of vitamin B12 (cobalamin) within the bodies. Bovine Transcobalamin-2 is encoded by the TCN2 gene in cattle. In cow's milk, B12 is evenly distributed between the whey and casein micellar fractions, bound to transcobalamin in the whey and coordinated to histidine residues in the caseins.

Target/Biomarker Bovine TCN2

Target Synonym transcobalamin 2; transcobalamin-2; TC II; TC-2; TCII; transcobalamin II; transcobalamin II; macrocytic anemia

Gene ID 281518

UniProt ID Q9XSC9

Shipping and Storage

This product is shipped with gel ice packs. It is recommended to store at 2-8 °C (Up to 6 months).

Documents

Datasheet

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

Gebreyesus, G. et al. Vitamin B(12) and transcobalamin in bovine milk: Genetic variation and genome-wide association with loci along the genome. JDS communications. 2021, 2: 127-131.