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Rabbit Anti-GLT8D1 antibody
Rabbit Anti-GLT8D1 antibody
MGC94018; Da2 24; GALA4A; Glycosyltransferase 8 domain containing 1; Glycosyltransferase 8 domain-containing protein 1; Glycosyltransferase AD 017; MSTP139; GL8D1_HUMAN.
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  • NO.:SL9555R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Pig,Horse,Rabbit,Sheep,)
    Applications:ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name GLT8D1
Chinese Name 糖基转移酶8结构域1抗体
Alias MGC94018; Da2 24; GALA4A; Glycosyltransferase 8 domain containing 1; Glycosyltransferase 8 domain-containing protein 1; Glycosyltransferase AD 017; MSTP139; GL8D1_HUMAN.  
Research Area Tumour  Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Pig, Horse, Rabbit, Sheep, )
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 42kDa
Cellular localization The cell membrane 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human GLT8D1: 201-300/371 
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 GLT8D1 is a 371 amino acid single-pass type II transmembrane protein that is expressed by a gene residing on human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. There are two isoforms of GLT8D1 that are produced as a result of alternative splicing events.

Subcellular Location:
Membrane; Single pass type II membrane protein

Similarity:
Belongs to the glycosyltransferase 8 family.

SWISS:
Q68CQ7

Gene ID:
55830

Database links:

Entrez Gene: 55830 Human

Entrez Gene: 76485 Mouse

Entrez Gene: 306253 Rat

SwissProt: Q68CQ7 Human

SwissProt: Q6NSU3 Mouse

SwissProt: Q6AYF6 Rat

Unigene: 297304 Human

Unigene: 8766 Mouse

Unigene: 91636 Rat



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