R

FH (PT1744R) PT™ Rabbit mAb

-YM9586

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Catalog: YM9586
Size
Price
Status
Qty.
200μL
$600.00
3 weeks

0

100μL
$340.00
3 weeks

0

40μL
$190.00
3 weeks

0

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Collected

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Main Information
Target

FH

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, IHC, IF, IP, ELISA

MW

55kD (Calculated)

49kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
IHC 1:200-1:1000; WB 1:2000-1:10000; IF 1:200-1:1000; ELISA 1:5000-1:20000; IP 1:50-1:200;
Formulation
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Specificity
Endogenous
Purification
Protein A
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
MW(Calculated)
55kD
MW(Observed)
49kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
PT1744R
Isotype
IgG,Kappa
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Antigen&Target Information
Specificity:
Endogenous
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Gene Name:
FH
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Protein Name:
Fumarate hydratase, mitochondrial
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Other Name:
Fumarate hydratase, mitochondrial ;
Fumarase ;
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Database Link:
Organism Gene ID SwissProt
Human 2271; P07954;
Mouse 14194; P97807;
Rat P14408;
Background:
The protein encoded by this gene is an enzymatic component of the tricarboxylic acid (TCA) cycle, or Krebs cycle, and catalyzes the formation of L-malate from fumarate. It exists in both a cytosolic form and an N-terminal extended form, differing only in the translation start site used. The N-terminal extended form is targeted to the mitochondrion, where the removal of the extension generates the same form as in the cytoplasm. It is similar to some thermostable class II fumarases and functions as a homotetramer. Mutations in this gene can cause fumarase deficiency and lead to progressive encephalopathy. [provided by RefSeq, Jul 2008],
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Function:
Catalytic activity:(S)-malate = fumarate + H(2)O.,Disease:Defects in FH are the cause of fumarase deficiency (FD) [MIM:606812]; also known as fumaricaciduria. FD is characterized by progressive encephalopathy, developmental delay, hypotonia, cerebral atrophy and lactic and pyruvic acidemia.,Disease:Defects in FH are the cause of hereditary leiomyomatosis and renal cell cancer (HLRCC) [MIM:605839].,Disease:Defects in FH are the cause of multiple cutaneous and uterine leiomyomata (MCUL1) [MIM:150800]. MCUL1 is an autosomal dominant condition in which affected individuals develop benign smooth muscle tumors (leiomyomata) of the skin. Affected females also usually develop leiomyomata of the uterus (fibroids).,Function:Also acts as a tumor suppressor.,miscellaneous:There are 2 substrate binding sites: the catalytic A site, and the non-catalytic B site that may play a role in the transfer of substrate or product between the active site and the solvent. Alternatively, the B site may bind allosteric effectors.,pathway:Carbohydrate metabolism; tricarboxylic acid cycle.,PTM:Isoform Cytoplasmic is acetylated at position 2.,similarity:Belongs to the class-II fumarase/aspartase family. Fumarase subfamily.,subunit:Homotetramer.,
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Cellular Localization:
[Isoform Mitochondrial]: Mitochondrion .; [Isoform Cytoplasmic]: Cytoplasm, cytosol . Nucleus . Chromosome . Translocates to the nucleus in response to DNA damage: localizes to DNA double-strand breaks (DSBs) following phosphorylation by PRKDC. .
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Research Areas:
>>Citrate cycle (TCA cycle) ;
>>Pyruvate metabolism ;
>>Metabolic pathways ;
>>Carbon metabolism ;
>>Cushing syndrome ;
>>Pathways in cancer ;
>>Renal cell carcinoma
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Catalog: YM9586
Size
Price
Status
Qty.
200μL
$600.00
3 weeks

0

100μL
$340.00
3 weeks

0

40μL
$190.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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