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C21orf70 Polyclonal Antibody

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. The C21orf70 gene product has been provisionally designated C21orf70 pending further characterization.

Synonyms

Chromosome 21 open reading frame 70; CU070_HUMAN; Hypothetical protein LOC85395; PRED56; Uncharacterized protein C21orf70.

Gene ID

85395

Swiss Prot

Q9NSI2

Host

Rabbit

Cross Reactivity

Human

Immunogen

51-150/230

Target

C21orf70

Clonality

Polyclonal

Isotype

IgG

Conjugation

Unconjugated

Source

KLH conjugated synthetic peptide derived from human C21orf70

Applications

IHC-P, IHC-F, IF

Purification

Purified by Protein A.

Concentration

1µg/µl

Dilution

IHC-P (IHC-P=1:100-500), IHC-F (IHC-F=1:100-500), IF (IF=1:100-500)

Buffer

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

Modification

Unmodified

Storage Conditions

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

Gene ID URL

85395

Frequently Asked Questions

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