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WBS16 Antibody

Product Specifications

Background

This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq].

NCBI Gene ID

81554

Swiss Prot

Q96I51

Accession Number

Q96I51

Host

Rabbit

Reactivity

Human, Hamster

Immunogen

This WBS16 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 15-44 amino acids from the N-terminal region of human WBS16.

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Cell Cycle

Purification

This antibody is purified through a protein A column, followed by peptide affinity purification.

Concentration

Batch dependent

Buffer

Supplied in PBS with 0.09% (W/V) sodium azide.

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

Store at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Calculated Molecular Weight

50 kDa

Fragment

Rabbit Ig

Applications Notes

For WB starting dilution is: 1:1000

Symbol

WBSCR16

NCBI Official Name

Williams-Beuren syndrome chromosomal region 16 protein

NCBI Organism

Homo sapiens

Background Reference 01

Merla, G., et al. Hum. Genet. 110 (5) :429-438 (2002)

Other Product Names

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

Tested Applications

WB

Protein ID

116242843

Physical Properties

Liquid

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