FASTKD1 Polyclonal Antibody | G-AB-11666

FASTKD1 Polyclonal Antibody | G-AB-11666 | Gentaur Antibodies

Overview: The second largest human chromosome, 2 consists of 237 million bases encoding over 1, 400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

Category Type: Polyclonal Antibody

Research Areas: Cell Biology

Synonyms: FASTKD1

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID: 79675

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human FASTKD1 (NP_078898.3) .

Clone #:

Conjugation: Unconjugated

Swissprot: Q53R41

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: IHC

Dilution: IHC 1:50-1:200

Storage: Store at -20°C. Avoid freeze / thaw cycles.

FASTKD1 Polyclonal Antibody DataSheet