FAH Monoclonal antibody

FAH Monoclonal Antibody for IF/ICC, WB, ELISA

Host / Isotype

Mouse / IgG1

Reactivity

Human, pig, rat, mouse

Applications

IF/ICC, WB, ELISA

Conjugate

Unconjugated

CloneNo.

2F8E11

Cat No : 67986-1-Ig

Print datasheet

Synonyms

Beta diketonase, FAA, FAH, Fumarylacetoacetase, Fumarylacetoacetate hydrolase



经过测试的应用

Positive WB detected inLNCaP cells, pig liver tissue, rat liver tissue, mouse liver tissue, HepG2 cells, Jurkat cells, K-562 cells
Positive IF detected inHepG2 cells
Planning an IF experiment? We recommend our CoraLite® Plus 488 and CoraLite®555 conjugated versions of this antibody.

推荐稀释比

ApplicationDilution
Western Blot (WB)WB : 1:5000-1:50000
Immunofluorescence (IF)IF : 1:200-1:800
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.

产品信息

67986-1-Ig targets FAH in WB, IF, ELISA applications and shows reactivity with Human, pig, rat, mouse samples.

Tested Applications IF/ICC, WB, ELISA
Tested Reactivity Human, pig, rat, mouse
Immunogen FAH fusion protein Ag6704 种属同源性预测
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Full Name fumarylacetoacetate hydrolase (fumarylacetoacetase)
Synonyms Beta diketonase, FAA, FAH, Fumarylacetoacetase, Fumarylacetoacetate hydrolase
Calculated Molecular Weight 46 kDa
Observed Molecular Weight 40-45 kDa
GenBank Accession NumberBC002527
Gene Symbol FAH
Gene ID (NCBI) 2184
RRIDAB_2918735
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
UNIPROT IDP16930
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

FAH is also named as FAA(fumarylacetoacetase), the last enzyme in tyrosine degradation, functionally important in the liver and kidney(PMID:8473520). FAH is a metabolic enzyme catalyzing the last step of tyrosine and phenylalanine catabolism: the hydrolysis of fumarylacetoacetate into acetoacetate and fumarate. In humans, deficiency of this activity is associated with the metabolic disease hereditary tyrosinaemia type I, which is also known as hepatorenal tyrosinaemia(PMID:17768357).

实验方案

Product Specific Protocols
WB protocol for FAH antibody 67986-1-IgDownload protocol
IF protocol for FAH antibody 67986-1-IgDownload protocol
Standard Protocols
Click here to view our Standard Protocols