DDX3Y antibody (AA 70-316)

Catalog No. ABIN1886628

The Rabbit Polyclonal anti-DDX3Y antibody (ABIN1886628) specifically detects DDX3Y in WB and IF. The antibody is reactive with Human samples.

Quick Overview for DDX3Y antibody (AA 70-316) (ABIN1886628)

Target: DDX3Y (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 3, Y-Linked (DDX3Y))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DDX3Y antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Product Details anti-DDX3Y Antibody

Binding Specificity: AA 70-316

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 70 and 316 of DDX3Y

Application Details

Application Notes: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunofluorescence: 1.100-1.200

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Preservative: Thimerosal (Merthiolate)

Precaution of Use: Biohazard Informations: This product contains thimerosal which is hazardous.

Storage: 4 °C/-20 °C

Storage Comment: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Target Details for DDX3Y

Target: DDX3Y (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 3, Y-Linked (DDX3Y))

Alternative Name: DDX3Y

Background: DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases.They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly.Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division.This gene encodes a DEAD box protein, and it has a homolog on the X chromosome.The gene mutation causes male infertility, Sertoli cell-only syndrome or severe hypospermatogenesis, suggesting that this gene plays a key role in the spermatogenic process.Alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq]

Molecular Weight: 73 kDa

Gene ID: 8653

NCBI Accession: NP_004651, NM_004660