Description:

Size: 100ul

Catalog no.: bs-5064R-A350

Price: 380 EUR

Product details

Modification Site

None

Target Antigen

HADHA

Gene ID Number

116535

Tested applications

IF(IHC-P)

French translation

anticorps

Clonality

Polyclonal

Modification

Unmodified

Concentration

1ug per 1ul

Excitation emission

343nm/442nm

Conjugated with

ALEXA FLUOR® 350

Crossreactivity

Human, Mouse, Rat

Clone

Polyclonal antibody

Recommended dilutions

IF(IHC-P)(1:50-200)

Purification

Purified by Protein A.

Conjugation

Alexa Fluor,ALEXA FLUOR 350

Category

Conjugated Primary Antibodies

Host Organism

Rabbit (Oryctolagus cuniculus)

Also known as

Anti-HADHA PAb ALEXA FLUOR 350

Specificity

This is a highly specific antibody against HADHA.

Long name

HADHA Polyclonal Antibody, ALEXA FLUOR 350 Conjugated

Cross-reactive species details

Due to limited amount of testing and knowledge, not every possible cross-reactivity is known.

Source

This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human HADHA

Storage conditions

Store this antibody in aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% sodium azide. Keep refrigerated at 2 to 8 degrees Celcius for up to one year.

Properties

For facs or microscopy Alexa 1 conjugate.Alexa Fluor 350 conjugates can be used in multi-color flow cytometry with FACS's equipped with a second red laser or red diode.If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies. ALEXA FLUOR they should be stored frozen at - 24°C for long term storage and for short term at + 5°C.

Background of the antigen

This gene encodes the alpha subunit of the mitochondrial trifunctional protein, which catalyzes the last three steps of mitochondrial beta-oxidation of long chain fatty acids. The mitochondrial membrane-bound heterocomplex is composed of four alpha and four beta subunits, with the alpha subunit catalyzing the3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase activities. Mutations in this gene result in trifunctional protein deficiency or LCHAD deficiency. The genes of the alpha and beta subunits of the mitochondrial trifunctional protein are located adjacent to each other in the human genome in a head-to-head orientation. [provided by RefSeq, Jul 2008].

Synonyms

HADHA; LCHAD; ECHA; GBP; HADH; LCEH; LCHAD; MTPA; TP-ALPHA; 3 ketoacyl Coenzyme A CoA thiolase alpha subunit; 3 oxoacyl CoA thiolase; 78 kDa gastrin binding protein; GBPv HADHv Hydroxyacyl Coenzyme A dehydrogenase/3 ketoacyl Coenzyme A thiolase/enoyl Coenzyme A hydratase trunctional protein alpha subunit; LCHAD; Mitochondrial long chain 2 enoyl Coenzyme A CoA hydratase alpha subunit; Mitochondrial long chain L 3 hydroxyacyl Coenzyme A dehydrogenase alpha; Mitochondrial trunctional enzyme alpha subunit; Mitochondrial trunctional protein alpha subunit; MTPA; Thiolase/enoyl Coenzyme A hydratase trunctional protein alpha subunit; TP ALPHA; Trunctional enzyme subunit alpha mitochondrial precursor.