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Rabbit Anti-GSG1L/Biotin Conjugated antibody
Rabbit Anti-GSG1L/Biotin Conjugated antibody
Germ cell-specific gene 1-like protein; GSG1-like protein; GSG1L; GSG1L_HUMAN; KTSR5831; MGC18079; PRO19651.
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  • NO.:SL16335R-Bio
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Mouse,Rat,(predicted: Human,Dog,Pig,Cow,)
    Applications:WB ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name Anti-GSG1L/Biotin
Chinese Name 生物素标记的生殖细胞相关1样蛋白抗体
Alias Germ cell-specific gene 1-like protein; GSG1-like protein; GSG1L; GSG1L_HUMAN; KTSR5831; MGC18079; PRO19651.  
Research Area Cell biology  immunology  Developmental biology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Mouse, Rat,  (predicted: Human, Dog, Pig, Cow, )
Applications WB=1:50-200 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 37kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human GSG1L
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Product Detail background:
GSG1L is a 331 amino acid multi-pass membrane protein belonging to the GSG1 family. Existing as four alternatively spliced isoforms, GSG1L is encoded by a gene located on human chromosome 16, which encodes over 900 genes, comprises nearly 3% of the human genome and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. A rare disorder known as Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Subcellular Location:
Membrane.

Similarity:
Belongs to the GSG1 family.

Database links:

Entrez Gene: 146395 Human

Entrez Gene: 269994 Mouse

Entrez Gene: 499263 Rat

SwissProt: Q6UXU4 Human

SwissProt: D3Z7H4 Mouse

SwissProt: D3ZK93 Rat

SwissProt: Q4V922 Zebrafish

Unigene: 91910 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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