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Rabbit Anti-SPATA5 antibody
Rabbit Anti-SPATA5 antibody
AFG2; ATPase family gene 2 homolog; ATPase family protein 2 homolog; SPAF; Spermatogenesis associated 5; Spermatogenesis associated factor SPAF; Spermatogenesis-associated factor protein.
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  • NO.:SL17631R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Dog,Pig,Cow,)
    Applications:ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name SPATA5
Chinese Name 精子发生相关蛋白2抗体
Alias AFG2; ATPase family gene 2 homolog; ATPase family protein 2 homolog; SPAF; Spermatogenesis associated 5; Spermatogenesis associated factor SPAF; Spermatogenesis-associated factor protein.  
Research Area Cell biology  Developmental biology  Stem cells  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, )
Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 98kDa
Cellular localization cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human SPATA5: 801-893/893 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail SPATA5 is an 893 amino acid protein that localizes to cytoplasm and mitochondrion, and may be involved in morphological and functional mitochondrial transformations during spermatogenesis. Existing as three alternatively spliced isoforms, SPATA5 belongs to the AAA ATPase family and the AFG2 subfamily. The gene that encodes SPATA5 consists of more than 396,000 bases and maps to human chromosome 4q28.1. Housing nearly 900 genes, chromosome 4 represents approximately 6% of the human genome and is associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

Function:
May be involved in morphological and functional mitochondrial transformations during spermatogenesis.

Subcellular Location:
Cytoplasmic and Mitochondrial

Similarity:
Belongs to the AAA ATPase family. AFG2 subfamily.

SWISS:
Q8NB90

Gene ID:
166378

Database links:

Entrez Gene: 166378 Human

Entrez Gene: 57815 Mouse

Entrez Gene: 361935 Rat

SwissProt: Q8NB90 Human

SwissProt: Q3UMC0 Mouse



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