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C21orf59 Polyclonal Antibody, AbBy Fluor™ 405 Conjugated

Selected Variant

bs-15126R-BF405

Size: 100 µL

Product Specifications

Background

The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.

Synonyms

C21orf48; C21orf59; Chromosome 21 open reading frame 59; CU059_HUMAN; FLJ20467; FLJ37137; FLJ40247; Uncharacterized protein C21orf59.

Gene ID

56683

Cellular Locus

Cytoplasm, Nucleus

Host

Rabbit

Immunogen

151-250/290

Target

C21orf59

Clonality

Polyclonal

Isotype

IgG

Conjugation

AbBy Fluor™ 405

Source

KLH conjugated synthetic peptide derived from human C21orf59

Applications

WB, IF (IHC-P), IF (IHC-F), IF (ICC)

Purification

Purified by Protein A.

Excitation Emission

401nm/421nm

Concentration

1µg/µl

Dilution

WB (1:300-5000), IF (IHC-P) (1:50-200), IF (IHC-F) (1:50-200), IF (ICC) (1:50-200)

Buffer

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Modification

Unmodified

Storage Conditions

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Gene ID URL

56683

Predicted Cross Reactivity

Human, Mouse, Rat, Cow, Sheep, Pig, Horse

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