LSMEM1 antibody (AA 31-100) (AbBy Fluor® 488)
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- Target See all LSMEM1 (C7ORF53) Antibodies
- LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))
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Binding Specificity
- AA 31-100
- Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This LSMEM1 antibody is conjugated to AbBy Fluor® 488
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Predicted Reactivity
- Human,Mouse,Rat,Dog
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C7orf53
- Isotype
- IgG
- Top Product
- Discover our top product C7ORF53 Primary Antibody
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- Application Notes
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))
- Alternative Name
- C7orf53 (C7ORF53 Products)
- Synonyms
- C7orf53 antibody, Gm889 antibody, C4H7orf53 antibody, C1H7orf53 antibody, C7ORF53 antibody, leucine rich single-pass membrane protein 1 antibody, leucine-rich single-pass membrane protein 1 antibody, LSMEM1 antibody, Lsmem1 antibody
- Background
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Synonyms: C7orf53, CG053_HUMAN, Chromosome 7 open reading frame 53, Coiled-coil domain-containing transmembrane protein C7orf53.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf53 gene product has been provisionally designated C7orf53 pending further characterization.
- Gene ID
- 286006
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