TDRP/C8orf42 antibody (AA 51-150) (FITC)
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- Target See all TDRP/C8orf42 (TDRP) Antibodies
- TDRP/C8orf42 (TDRP) (Testis Development Related Protein (TDRP))
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Binding Specificity
- AA 51-150
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Reactivity
- Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This TDRP/C8orf42 antibody is conjugated to FITC
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Rat
- Predicted Reactivity
- Human,Mouse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C8orf42
- Isotype
- IgG
- Top Product
- Discover our top product TDRP 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
- TDRP/C8orf42 (TDRP) (Testis Development Related Protein (TDRP))
- Alternative Name
- C8orf42 (TDRP Products)
- Synonyms
- C8orf42 antibody, Inm01 antibody, TDRP1 antibody, TDRP2 antibody, 2610019F03Rik antibody, c8orf42 antibody, testis development related protein antibody, testis development related protein L homeolog antibody, TDRP antibody, Tdrp antibody, tdrp.L antibody
- Background
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Synonyms: C8orf42, TDRP_HUMAN, Protein INM01, Protein TDRP, Uncharacterized protein C8orf42.
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 C8orf42 gene product has been provisionally designated C8orf42 pending further characterization.
- Gene ID
- 157695
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