FAM91A1 antibody (AA 335-440) (Biotin)
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- Target See all FAM91A1 products
- FAM91A1 (Family with Sequence Similarity 91, Member A1 (FAM91A1))
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Binding Specificity
- AA 335-440
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This FAM91A1 antibody is conjugated to Biotin
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Predicted Reactivity
- Human,Mouse,Rat,Chicken
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FAM91A1
- Isotype
- IgG
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- Application Notes
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 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 for 12 months.
- Expiry Date
- 12 months
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- Target
- FAM91A1 (Family with Sequence Similarity 91, Member A1 (FAM91A1))
- Alternative Name
- FAM91A1 (FAM91A1 Products)
- Synonyms
- AV220772 antibody, BC033609 antibody, Fam91a1 antibody, SKIN antibody, mKIAA0493 antibody, MGC63609 antibody, zgc:63609 antibody, family with sequence similarity 91, member A1 antibody, family with sequence similarity 91 member A1 antibody, Fam91a1 antibody, FAM91A1 antibody, fam91a1 antibody
- Background
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Synonyms: FAM91A1, Family with sequence similarity 91 member A1, FLJ23790, Hypothetical protein LOC157769, LOC157769, F91A1_HUMAN.
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 FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.
- Gene ID
- 157769
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