Alexa Fluor 488 anti-Bax Antibody anti-Bax - 2D2,BioLegend,633603

Clone 2D2 has been shown to be useful for Western blotting1, immunoprecipitation2, immunofluorescence3and immunohistochemical staining3of formalin-fixed and paraffin-embedded tissue sections. This antibody does not cross-react with Bcl-2 or Bcl-XLproteins.Clone 2D2 does not show specificity for mouse BAX.

Host

Mouse

Reactivity

Human

Application

ICFC - Quality tested

Platform ID

BAB614495689

BioLegend

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Contact

Tel: 1-858-455-9588
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Product Specifications
Scientific Background

Specifications

NameAlexa Fluor 488 anti-Bax Antibody anti-Bax - 2D2
Cat. No.633603
HostMouse
RRIDAB_2562171 (BioLegend Cat. No. 633603)AB_2562172 (BioLegend Cat. No. 633604)
IsotypeMouse IgG1, κ
ReactivityHuman
ApplicationICFC - Quality tested
ClonalityMonoclonal
Clone Number2D2
Concentration0.5 mg/ml
TargetBax
ImmunogenAmino acids 3-16 of human Bax protein
PurityThe antibody was purified by affinity chromatography and conjugated with Alexa Fluor® 488 under optimal conditions.
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
StorageThe antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light.Do not freeze.
Regulatory StatusResearch Use Only

Scientific Background

Bax is a 21 kD pro-apoptotic protein known to regulate apoptosis. Bax is found in the cytoplasm, mitochondria, and nucleus and is highly expressed in hematopoietic stem cells, ovaries, and lymph nodes. Bax binds the anti-apoptotic protein Bcl-2 as a heterodimer or forms homodimers. The relative levels of pro-apoptotic proteins such as Bax and anti-apoptotic proteins such as Bcl-2 determines whether cell death will occur following an apoptotic stimulus. Bax accelerates the opening of mitochondrial VDAC altering membrane potential and allowing cytochrome c to pass out of the mitochondria into the cytosol to initiate downstream caspase activation. p53 can transcriptionally activate the Bax gene to induce apoptosis. Bax has been shown to be mutated in some human cancers.

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