CDSN Antilichaam

This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. The encoded protein undergoes a series of cleavages during corneocyte maturation. This gene is highly polymorphic in human populations, and variation has been associated with skin diseases such as psoriasis, hypotrichosis and peeling skin syndrome. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6.

1041

Q15517

Human, Mouse, Rat

A synthetic peptide corresponding to a sequence within amino acids 100-200 of human CDSN (NP_001255.3) .

Unconjugated

Primary Antibodies

Cell Cycle, Signal Transduction

Affinity purification

BxPC-3

Batch dependent

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

None

Blue Ice

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

Observed: 52kDa

IgG

WB: 1:500 - 1:2000

CDSN

A-431

NIH/3T3

Mouse skin

Mouse skeletal muscle

Rat skin

Corneodesmosin

Homo sapiens

CDSN, corneodesmosin, D6S586E, HTSS, S, differentiated keratinocyte S protein

WB

Liquid