0 products, total $0.+86-400-890-9989      Login |  Register 中文한국어

Browse By Molecule:

Your Position: Home > Antibody > Rabbit MAb Antibody > Transferrin / TF Antibody

Transferrin / TF Antibody PDF Download

Catalog Size (Price) Quantity In Stock Operation Other Information
11019-R101
  YES          

Transferrin / TF Antibody Datasheet

  Order or Inquire for Transferrin / TF Antibody product
  Detection limit is 2 ng/lane in WB
  Detection limit is 0.00245 ng/well in ELISA
 

Transferrin / TF Antibody Product Information

Immunogen :

Recombinant Human Transferrin / TF protein (Catalog#11019-H08H)

Antibody Type : Rabbit Monoclonal Antibody ( Rabbit mAb Service Platform )

Clone ID :

101

Ig Type :

Rabbit IgG

Formulation : 0.2 μm filtered solution in PBS with 5% trehalose
Preparation :

This antibody was obtained from a rabbit immunized with purified, recombinant Human Transferrin / TF (rh Transferrin / TF; Catalog#11019-H08H; NP_001054.1; Met 1-Pro 698).

Transferrin / TF Antibody Usage Guide

Specificity :

Human Transferrin / TF

Western blot : This antibody can be used at 1-2 μg/mL with the appropriate secondary reagents to detect Human Transferrin / TF in WB. Using a DAB detection system, the detection limit for Human Transferrin / TF is approximately 2 ng/lane under non-reducing conditions. Use of this antibody under reducing conditions is not recommended.
Direct ELISA : This antibody can be used at 0.1-0.2 μg/mL with the appropriate secondary reagents to detect Human Transferrin / TF. The detection limit for Human Transferrin / TF is approximately 0.00245 ng/well.
Storage : This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -70℃. Preservative-Free.
Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.

Transferrin / TF Antibody Related Products & Topics

Related Areas:

Proteins:

Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
Transferrin Human Transferrin Protein, Recombinant 11019-H08H
Transferrin Sus scrofa (Pig) Transferrin Protein, Recombinant 13656-W02H
Transferrin Sus scrofa (Pig) Transferrin Protein, Recombinant 13656-W08H

Antibodies:

Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Human
Transferrin
ELISA, IHC-P Transferrin / TF Antibody 11019-MM03
Human
Transferrin
WB, ELISA Mouse Monoclonal Antibody 11019-MM06
Human
Transferrin
WB, ELISA Rabbit Polyclonal Antibody 11019-RP01
Human
Transferrin
WB, ELISA Rabbit Polyclonal Antibody (Antigen Affinity Purified) 11019-RP02
Human
Transferrin
WB, ELISA Rabbit Monoclonal Antibody 11019-R101

Transferrin / TF Antibody Background

Transferrin, also known as Serotransferrin, Beta-1 metal-binding globulin, TF, is a secreted protein which belongs to thetransferrin family. It is expressed by the liver and secreted in plasma and contains two transferrin-like domains. Transferrins are iron binding transport proteins which can bind two Fe3+ions in association with the binding of an anion, usually bicarbonate. It is responsible for the transport of iron from sites of absorption and heme degradation to those of storage and utilization. Serum transferrin may also have a further role in stimulating cell proliferation. When a transferrin protein loaded with iron encounters atransferrin receptoron the surface of acell, it binds to it and, as a consequence, is transported into the cell in avesicle. Transferrin is aglycoproteinthat binds iron very tightly but reversibly. Although iron bound to transferrin is less than 0.1% (4 mg) of the total body iron, it is the most important iron pool, with the highest rate of turnover (25 mg/24 h). Defects in transferrin are the cause of a transferrinemia (ATRAF) which is rare autosomal recessive disorder characterized by iron overload and hypochromic anemia. Transferrin is also associated with the innate immune system.

References

  1. Cheng Y, et al., 2004, Cell116 (4): 565-76.
  2. St. Edward's University. 2005-07-18. Retrieved 2009-04-24.
  3. Hafenstein S, et al., 2007,PNAS. 104 (16): 6585-9.