FKBP14 Polyclonal antibody
FKBP14 Polyclonal Antibody for WB, IHC, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human
Applications
WB, IHC, ELISA and More (1)
Conjugate
Unconjugated
验证数据展示
经过测试的应用
Positive WB detected in | HEK-293 cells, HeLa cells, human brain tissue |
Positive IHC detected in | human ovary cancer tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
推荐稀释比
Application | Dilution |
---|---|
Western Blot (WB) | WB : 1:500-1:2400 |
Immunohistochemistry (IHC) | IHC : 1:50-1:500 |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
发表文章中的应用
WB | See 3 publications below |
IF | See 3 publications below |
产品信息
15884-1-AP targets FKBP14 in WB, IHC, IF, ELISA applications and shows reactivity with human samples.
Tested Applications | WB, IHC, ELISA Application Description |
Cited Applications | WB, IF |
Tested Reactivity | human |
Cited Reactivity | human |
Immunogen | FKBP14 fusion protein Ag8668 种属同源性预测 |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Full Name | FK506 binding protein 14, 22 kDa |
Synonyms | FKBP-22, FKBP22, FKBP-14, FK506-binding protein 14, EC:5.2.1.8 |
Calculated Molecular Weight | 211 aa, 24 kDa |
Observed Molecular Weight | 28 kDa |
GenBank Accession Number | BC005206 |
Gene Symbol | FKBP14 |
Gene ID (NCBI) | 55033 |
RRID | AB_2102702 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Antigen affinity purification |
UNIPROT ID | Q9NWM8 |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
背景介绍
实验方案
Product Specific Protocols | |
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WB protocol for FKBP14 antibody 15884-1-AP | Download protocol |
IHC protocol for FKBP14 antibody 15884-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |
发表文章
Species | Application | Title |
---|---|---|
Am J Hum Genet Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss. | ||
Sci Rep The novel missense mutation Met48Lys in FKBP22 changes its structure and functions. | ||
Hum Mutat Kyphoscoliotic Ehlers-Danlos syndrome caused by pathogenic variants in FKBP14: Further insights into the phenotypic spectrum and pathogenic mechanisms | ||
Int J Mol Sci Local Net Charge State of Collagen Triple Helix Is a Determinant of FKBP22 Binding to Collagen III |