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Antibody used in IHC on Human kidney.
Antibody used in WB on Human HepG2 at 1.25 ug/ml.
Antibody used in IHC on Human kidney.

FKBP6 Antibody

CATALOG NUMBER: 29-825

Clonality:
Polyclonal
Tested Applications:
ELISA, IHC, WB
Host Species:
Rabbit
Species Reactivity:
Dog, Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Dog, Human, Mouse, Rat
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FKBP6.
Conjugate:
Unconjugated
Tested Applications:
ELISA, IHC, WB
Application Note:
FKBP6 antibody can be used for detection of FKBP6 by ELISA at 1:1562500. FKBP6 antibody can be used for detection of FKBP6 by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Cat. No. 1211 - HepG2 Cell Lysate
Predicted Molecular Weight:
53 kDa, 53 kDa
Purification:
Antibody is purified by protein A chromatography method.
Clonality:
Polyclonal
Physical State:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store FKBP6 antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
FKBP6
Additional Names:
FKBP6, FKBP36, MGC87179, PPIase
Protein Accession Number:
NP_003593
Protein Gi Number:
146229346
Ncbi Gene Id Number:
8468
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
FKBP6 is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. FKBP6 is a cis-trans prolyl isomerase that binds to the immunosuppressants FK506 and rapamycin.This gene encodes a member of the interferon regulatory transcription factor (IRF) family. Family members share a highly-conserved N-terminal helix-turn-helix DNA-binding domain and a less conserved C-terminal protein-binding domain. Mutations in this gene can cause van der Woude syndrome and popliteal pterygium syndrome. This protein is involved in palate formation.
Background Reference 1:
Ye, X.Q., (2005) Int. J. Mol. Med. 16 (5), 851-856.

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

29-825

List Size:
100 ul

List Price:

$473.00

Datasheet
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