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DNAJC30 Antibody

Product Specifications

Background

This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.

NCBI Gene ID

84277

Swiss Prot

Q96LL9

Accession Number

Q96LL9

Host

Rabbit

Reactivity

Human

Immunogen

This DNAJC30 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 176-202 amino acids from the C-terminal region of human DNAJC30.

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Signal Transduction

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

26 kDa

Fragment

Rabbit Ig

Applications Notes

For WB starting dilution is: 1:1000

Symbol

DNAJC30

NCBI Official Name

DnaJ homolog subfamily C member 30

NCBI Organism

Homo sapiens

Background Reference 01

Lamesch, P., et al. Genomics 89 (3) :307-315 (2007)

Background Reference 02

Lehner, B., et al. Genome Res. 14 (7) :1315-1323 (2004)

Background Reference 03

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

Other Product Names

DnaJ homolog subfamily C member 30, Williams-Beuren syndrome chromosomal region 18 protein, DNAJC30, WBSCR18

Tested Applications

WB

Protein ID

24212614

Physical Properties

Liquid

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