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Rabbit Anti-SPATA5L1 antibody
Rabbit Anti-SPATA5L1 antibody
FLJ12286; MGC5347; SPA5L_HUMAN; SPATA5L1; Spermatogenesis-associated protein 5-like protein 1.
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  • NO.:SL17632R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,(predicted: Mouse,Rat,Dog,Rabbit,)
    Applications:WB ELISA
    concentration:1mg/ml
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Details

Product Name SPATA5L1
Chinese Name 精子发生相关蛋白5样蛋白1抗体
Alias FLJ12286; MGC5347; SPA5L_HUMAN; SPATA5L1; Spermatogenesis-associated protein 5-like protein 1.  
Research Area Cell biology  immunology  Developmental biology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human,  (predicted: Mouse, Rat, Dog, Rabbit, )
Applications WB=1:500-2000 ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 81kDa
Cellular localization cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human SPATA5L1: 221-320/753 
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 SPATA5L1 is a 753 amino acid protein belonging to the AAA ATPase family and AFG2 subfamily. Single nucleotide polymorphisms (SNPs) present in SPATA5L1 at the glycine amidinotransferase (GATM)-SPATA5L1 locus have been found to correlate with glomerular filtration rate (GFR), having significant implications for kidney disease research. SPATA5L1 localizes to cytoplasm and exists as three alternatively spliced isoforms. The gene encoding SPATA5L1 maps to human chromosome 15q21.1. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3% of the human genome. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

Subcellular Location:
Cytoplasm.

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

SWISS:
Q9BVQ7

Gene ID:
79029

Database links:

Entrez Gene: 533070 Cow

Entrez Gene: 79029 Human

SwissProt: A7YSY2 Cow

SwissProt: Q9BVQ7 Human

Unigene: 21280 Cow

Unigene: 369657 Human



Product Picture
Sample:
Panc-1(Human) Cell Lysate at 30 ug
Primary: Anti-SPATA5L1 (SL17632R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 81 kD
Observed band size: 81 kD

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