Product Name	C6orf192
Chinese Name	8号染色体开放阅读框192抗体
Alias	chromosome 6 open reading frame 192; hypothetical protein LOC116843; Uncharacterized MFS-type transporter C6orf192; S18B1_HUMAN.
literatures	Specific References  (1)     |     SL9530R has been referenced in 1 publications. [IF=16.174] Zhao Xiaohui. et al. Chemoproteomics reveals microbiota-derived aromatic monoamine agonists for GPRC5A. NAT CHEM BIOL. 2023 May;:1-10  WB ;  Human.   PubMed:37248411
Research Area	Tumour  Cell biology  immunology  Neurobiology
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	(predicted: Human, Mouse, Rat, Dog, Pig, Cow, Rabbit, Sheep, )
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	49kDa
Cellular localization	The cell membrane
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human C6orf192: 1-100/456 <Extracellular>
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	Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf192 gene product has been provisionally designated C6orf192 pending further characterization. Subcellular Location: Membrane; Multi-pass membrane protein. Similarity: Belongs to the major facilitator superfamily. SWISS: Q6NT16 Gene ID: 116843 Database links: Entrez Gene: 116843 Human SwissProt: Q6NT16 Human Unigene: 347144 Human
Product Picture	Sample: Large intestne (Mouse) Lysate at 40 ug Primary: Anti-C6orf192 (SL9530R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 49 kD Observed band size: 49 kD

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