FAM76B antibody (Cy5)
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- Target See all FAM76B products
- FAM76B (Family with Sequence Similarity 76, Member B (FAM76B))
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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 FAM76B antibody is conjugated to Cy5
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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 FAM76B
- 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
- FAM76B (Family with Sequence Similarity 76, Member B (FAM76B))
- Alternative Name
- FAM76B (FAM76B Products)
- Synonyms
- fa11h02 antibody, wu:fa11h02 antibody, zgc:73333 antibody, 2810485I05Rik antibody, C78303 antibody, RGD1311077 antibody, family with sequence similarity 76 member B antibody, family with sequence similarity 76, member B antibody, family with sequence similarity 76 member B S homeolog antibody, FAM76B antibody, fam76b antibody, fam76b.S antibody, Fam76b antibody
- Background
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Synonyms: Family with sequence similarity 76 member B, Hypothetical protein LOC143684, MGC33371, FA76B_HUMAN.
Background: With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
- Gene ID
- 143684
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