HSFY1 antibody

Catalog No. ABIN2854539

This anti-HSFY1 antibody is a Rabbit Polyclonal antibody detecting HSFY1 in WB. Suitable for Human.

Quick Overview for HSFY1 antibody (ABIN2854539)

Target: HSFY1 (Heat Shock Transcription Factor, Y-Linked 1 (HSFY1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HSFY1 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-HSFY1 Antibody

Cross-Reactivity: Mouse, Rat

Characteristics: Rabbit Polyclonal antibody to HSFY1+2 (heat shock transcription factor, Y-linked 1)
HSFY1+2 antibody

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human HSFY1+2. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: mouse testis , Rat testis

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

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

Target Details for HSFY1

Target: HSFY1 (Heat Shock Transcription Factor, Y-Linked 1 (HSFY1))

Alternative Name: heat shock transcription factor, Y-linked 1

Background: This gene encodes a member of the heat shock factor (HSF) family of transcriptional activators for heat shock proteins. This gene is a candidate gene for azoospermia, since it localizes to a region of chromosome Y that is sometimes deleted in infertile males. The genome has two identical copies of this gene within a palindromic region, this record represents the more centromeric copy. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Cellular Localization: Nucleus , Cytoplasm

Molecular Weight: 45 kDa

Gene ID: 86614