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COL4A5

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This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]

Derivation:
Mouse
Species Reactivity:
Human
Type:
IgG
Application:
ELISA, WB, Neut, FuncS
Derivation:
Mouse
Species Reactivity:
Human
Type:
Fab
Application:
FC, Neut, Funcs
Derivation:
Mouse
Species Reactivity:
Human
Type:
scFv
Application:
IF, FC, Biosensors, FuncS
Class:
Class I
Target:
COL4A5
Specificity:
Human
Peptide:
SLWGQPAEA
Conjugate:
PE
Class:
Class I
Target:
COL4A5
Specificity:
Human
Peptide:
SLWGQPAEA
Conjugate:
PE
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