C6orf192 antibody (AA 50-80)
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- Target See all C6orf192 Antibodies
- C6orf192 (Chromosome 6 Open Reading Frame 192 (C6orf192))
- Binding Specificity
- AA 50-80
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This C6orf192 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C6orf192
- Isotype
- IgG
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- Application Notes
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- 4 °C,-20 °C
- Storage Comment
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Expiry Date
- 12 months
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- Target
- C6orf192 (Chromosome 6 Open Reading Frame 192 (C6orf192))
- Alternative Name
- C6orf192 (C6orf192 Products)
- Synonyms
- C3H6orf192 antibody, SLC18B1 antibody, C6orf192 antibody, dJ55C23.6 antibody, 1110021L09Rik antibody, solute carrier family 18, subfamily B, member 1 antibody, solute carrier family 18 member B1 antibody, slc18b1 antibody, SLC18B1 antibody, Slc18b1 antibody
- Background
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Synonyms: C6orf192, dJ55C23.6, MFS-type transporter SLC18B1, Solute carrier family 18 member B1, SLC18B1
Background: 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.
- Gene ID
- 116843
- UniProt
- Q6NT16
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