WBSCR16 Antilichaam

This gene encodes a protein containing regulator of chromosome condensation 1-like repeats. The encoded protein may function as a guanine nucleotide exchange factor. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. Alternative splicing results in multiple transcript variants.

81554

Q96I51

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-230 of human WBSCR16 (NP_110425.2) .

Unconjugated

Primary Antibodies

Cell Cycle

Affinity purification

Raji

Batch dependent

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

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 50kDa

IgG

WB: 1:500 - 1:2000

WBSCR16

HeLa

LO2

Mouse liver

Rat liver

Williams-Beuren syndrome chromosomal region 16 protein

Homo sapiens

Williams-Beuren syndrome chromosomal region 16 protein, RCC1-like G exchanging factor-like protein, WBSCR16

WB

Liquid