KD-Validated HSD17B4 Mouse Monoclonal Antibody

KD-Validated HSD17B4 Mouse Monoclonal Antibody

Cat: KVAb00273
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,FCM,ICC

Reactivity:Human,Mouse
Conjugate:Unconjugated
Gene Name:HSD17B4
Category: KO&KD Validated Antibodies Tags: , , , , , , , , , , ,

Summary

Production Name

KD-Validated HSD17B4 Mouse Monoclonal Antibody

Description

KD-Validated antibody

Host

Mouse

Application

WB,FCM,ICC

Reactivity

Human,Mouse

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Mouse IgG2b

Clonality

Mouse mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

HSD17B4

Alternative Names

HSD17B4; Hydroxysteroid 17-Beta Dehydrogenase 4; SDR8C1; MFE-2; DBP; 17-Beta-Hydroxysteroid Dehydrogenase 4; 3-Alpha,7-Alpha,12-Alpha-Trihydroxy-5-Beta-Cholest-24-Enoyl-CoA Hydratase; Short Chain Dehydrogenase/Reductase Family 8C Member 1; Peroxisomal Multifunctional Enzyme Type 2; 17beta-Estradiol Dehydrogenase Type IV; Peroxisomal Multifunctional Protein 2; D-Bifunctional Protein, Peroxisomal; D-3-Hydroxyacyl-CoA Dehydratase; Beta-Hydroxyacyl Dehydrogenase; Multifunctional Protein 2; Beta-Keto-Reductase; 17-Beta-HSD IV; 17-Beta-HSD 4; MFP-2; Short Chain Dehydrogenase/Reductase Family 8C, Member 1; Epididymis Secretory Sperm Binding Protein; Hydroxysteroid (17-Beta) Dehydrogenase 4; Hydroxysteroid Dehydrogenase 4; D-Bifunctional Protein; EDH17B4; PRLTS1; MPF-2

Gene ID

3295

SwissProt ID

P51659

 

Application

Dilution Ratio

WB 1:400-1:2,000; FC 1:200-1:2,000; ICC 1:100-1:1,000

Molecular Weight

Calculated MW: 79.7kDa

 

Background

The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]

 

Research Area

Signal Transduction,Cancer,Cardiovascular,Metabolism

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