FAM135B antibody (AA 1080-1130) (AbBy Fluor® 488)
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- Target See all FAM135B products
- FAM135B (Family with Sequence Similarity 135, Member B (FAM135B))
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Binding Specificity
- AA 1080-1130
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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 FAM135B antibody is conjugated to AbBy Fluor® 488
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FAM135B
- Isotype
- IgG
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- Application Notes
- IF(IHC-P) 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
- FAM135B (Family with Sequence Similarity 135, Member B (FAM135B))
- Alternative Name
- FAM135B (FAM135B Products)
- Synonyms
- MGC81353 antibody, C8ORFK32 antibody, RGD1308133 antibody, 1700010C24Rik antibody, A830008O07Rik antibody, family with sequence similarity 135 member B antibody, family with sequence similarity 135 member B L homeolog antibody, family with sequence similarity 135, member B antibody, FAM135B antibody, fam135b.L antibody, Fam135b antibody
- Background
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Synonyms: C8ORFK32, Protein FAM135B, FAM135B
Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM135B gene product has been provisionally designated FAM135B pending further characterization.
- Gene ID
- 51059
- UniProt
- Q49AJ0
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