Search results for WBSCR22 antibody

Showing 1 – 10 of6products
WBSCR22 antibody Brand Logo
ID: BAB242751683

WBSCR22 antibody, Genetex, GTX105840

Host

Rabbit

Reactivity

Human, Mouse

Applications

WB ICC/IF IHC-P IP

Conjugation

Unconjugated

WBSCR22 antibody Brand Logo
ID: BAB636319002

WBSCR22 antibody, Genetex, GTX33582

Host

Rabbit

Reactivity

Human, Rat

Applications

WB ICC/IF IHC-P

Conjugation

Unconjugated

WBSCR22 Antibody (YA9318)
ID: BAB685477005

WBSCR22 Antibody (YA9318), MedChemexpress, HY-P89974

WBSCR22 Antibody (YA9318) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to WBSCR22.

Host

Mouse

Reactivity

human

Applications

WB, ICC/IF, IF-Tissue, IP, ELISA

Conjugation

Non-conjugated

Anti-WBSCR22 antibody Brand Logo
ID: BAB951266375

Anti-WBSCR22 antibody, Abcam, AB97911

Host

Rabbit

Reactivity

Human, Mouse

Applications

WB, IHC-P

Conjugation

Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody Brand Logo
ID: BAB232381951

Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody, Abbexa, abx031474

This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.

Host

Rabbit

Reactivity

Human

Applications

ELISA, WB

Conjugation

Unconjugated

Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody Brand Logo
ID: BAB721858154

Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody, Abbexa, abx005524

WBSCR22 Antibody is a Rabbit Polyclonal antibody against WBSCR22. This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.

Host

Rabbit

Reactivity

Human, Rat

Applications

ELISA, WB, IF/ICC

Conjugation

Unconjugated

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