FAM65B antibody (AA 201-300)

Catalog No. ABIN1714750

Product Details anti-FAM65B Antibody

Target: FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))

Binding Specificity: AA 201-300

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM65B antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM65B

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for FAM65B

Target: FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))

Alternative Name: FAM65B (FAM65B Products)

Synonyms: C6orf32 antibody, DIFF40 antibody, DIFF48 antibody, MYONAP antibody, PL48 antibody, 1700108N18Rik antibody, 6330500D04Rik antibody, AI225904 antibody, E430013J17Rik antibody, si:dkey-218n20.1 antibody, Ab2-162 antibody, RGD1306939 antibody, RHO family interacting cell polarization regulator 2 antibody, family with sequence similarity 65, member B antibody, ripor2 antibody, RIPOR2 antibody, Ripor2 antibody, FAM65B antibody

Background:

Synonyms: Ab2 162, C6orf32, DF48, FA65B_HUMAN, Fam65b, KIAA0386, PL48, Protein FAM65B.

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 C6orf32 gene product has been provisionally designated C6orf32 pending further characterization.

Gene ID: 9750

Pathways: Transition Metal Ion Homeostasis