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AHA-1 antibody [25F2.D9]

Anti-AHA-1 antibody [25F2.D9] used in IHC (Paraffin sections) (IHC-P). GTX48775
Anti-AHA-1 antibody [25F2.D9] used in Western Blot (WB). GTX48775
Anti-AHA-1 antibody [25F2.D9] used in Western Blot (WB). GTX48775

Cat. No. GTX48775

Host

 Rat

Clonality

 Monoclonal

Clone Name

 25F2.D9

Isotype

 IgG2a

Application

 WB, IHC-P, ELISA

Reactivity

 Human
Package
50 μg ($399)
See all AHA-1 products

APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.
Application Recommended Dilution
WB 1:1000
IHC-P 5-10 μg/mL
ELISA 1:20000
Not tested in other applications.

Calculated MW

38 kDa. ( Note )

PROPERTIES

Form

Liquid

Buffer

20mM Potassium Phosphate, 150mM NaCl

Preservative

No preservative

Storage

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

Concentration

1 mg/ml (Please refer to the vial label for the specific concentration.)

Antigen Species

Mouse

Immunogen

Full length recombinant mouse AHA1 protein followed by hybridoma development.

Purification

IgG fraction
This product is an IgG fraction antibody purified from tissue culture supernatant by Protein-G chromatography, followed by extensive dialysis against the buffer stated above.

Conjugation

Unconjugated

Note

For laboratory research use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.

Purchasers shall not, and agree not to enable third parties to, analyze, copy, reverse engineer or otherwise attempt to determine the structure or sequence of the product.

TARGET

Synonyms

AHA1, activator of heat shock protein ATPase 1 , BC023857 , p38

Cellular Localization

Cytoplasm, cytosol,Endoplasmic reticulum

Background

Activator of Hsp90 ATPase (AHA1) stimulates the inherent ATPase cycle of Hsp90, which is essential for its chaperone activity in vivo. The activation and/or stability of many of the key regulatory and signaling proteins of the eukaryotic cell depend on their interaction with the Hsp90 molecular chaperone. Hsp90 is assisted and regulated by co-chaperones that participate in an ordered series both to assist client-protein recruitment or release and to modulate progress through the ATPase coupled chaperone cycle. Structural analysis and mutagenesis show that binding of the N-terminal domain of AHA1 to Hsp90 promotes a conformational switch in the middle-segment catalytic loop (aa 370–390) of Hsp90 that exposes the catalytic Arg380 and enables its interaction with ATP in the N-terminal nucleotide-binding domain of the chaperone. Recent studies show that AHA1 modulates Hsp90-dependent stability of the folding of the cystic fibrosis transmembrane conductance regulator (CFTR) in the endoplasmic reticulum (ER). Down-regulation of AHA1 rescues misfolding of CFTR in cystic fibrosis.

Database

Research Area

DATA IMAGES

Anti-AHA-1 antibody [25F2.D9] used in IHC (Paraffin sections) (IHC-P). GTX48775

GTX48775 IHC-P Image

GeneTex's anti-AHA1 monoclonal antibody was used at a 5-10 μg/mL to detect AHA1 in the seminiferous tubule of human testis (40X) showing moderate staining. Leydig cells showed faint to moderate staining. Expression of AHA1 is reported in many epithelial and lymphatic tissues, with cytoplasmic localization. This antibody showed moderate cytoplasmic staining of a variety of epithelial tissues and lymphoid organs such as spleen and tonsil with minimal background staining. The image shows the localization of the antibody as the precipitated red signal, with a hematoxylin purple nuclear counterstain. Tissue was formalin-fixed and paraffin embedded.

Anti-AHA-1 antibody [25F2.D9] used in Western Blot (WB). GTX48775

GTX48775 WB Image

Western blot using GeneTex's anti-AHA1 monoclonal antibody shows detection of a band ~42 kDa in size corresponding to AHA1 in A431 whole cell lysate (lane 1) and MCF-7 whole cell lysate (lane 2). A control lane is shown where primary ahntibody was omitted from the incubation (lane C). Molecular weight markers are shown at the left. For best results, block the membrane overnight with 3% BSA in TBS followed by reaction with primary antibody diluted 1:1,000 and use HRP conjugated anti-Rabbit IgG secondary antibody diluted 1:20,000 in blocking buffer) for detection.

Anti-AHA-1 antibody [25F2.D9] used in Western Blot (WB). GTX48775

GTX48775 WB Image

WB analysis of various samples using GTX48775 AHA-1 antibody [25F2.D9].
Lane 1 : A431 whole cell lysate
Lane 2 : MCF-7 whole cell lysate
Lane C : Without primary antibody
Dilution : 1:1000

REFERENCE

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REVIEW

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Package List Price ($)
$ 399