FAM229B antibody (AA 21-80) (Cy5)

Catalog No. ABIN1705101

Product Details anti-FAM229B Antibody (Cy5)

Target: FAM229B (Family with Sequence Similarity 229, Member B (FAM229B))

Binding Specificity: AA 21-80

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM229B antibody is conjugated to Cy5

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Predicted Reactivity: Human,Mouse,Rat,Cow,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C6orf225

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

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

Target Details for FAM229B

Target: FAM229B (Family with Sequence Similarity 229, Member B (FAM229B))

Alternative Name: C6orf225 (FAM229B Products)

Synonyms: C6orf225 antibody, 1700025K23Rik antibody, C9H6orf225 antibody, family with sequence similarity 229 member B antibody, family with sequence similarity 229, member B antibody, FAM229B antibody, Fam229b antibody

Background:

Synonyms: C6orf225, F229B_HUMAN, UPF0731 protein C6orf225.

Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf225 gene product has been provisionally designated C6orf225 pending further characterization.

Gene ID: 619208