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  1. Alles ansehen
  2. Polyclonal

GTX04635

EDA antibody

Eine Lieferung in diese Region ist nicht möglich.

SKU:
GTX04635
Zusätzliche Namen:
ectodysplasin A , ECTD1 , ED1 , ED1-A1 , ED1-A2 , EDA-A1 , EDA-A2 , EDA1 , EDA2 , HED , HED1 , ODT1 , STHAGX1 , TNLG7C , XHED , XLHED
Anwendung:
WB
Konzentration:
0.5 mg/ml
Physischer Zustand:
Liquid
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Hersteller:
Genetex
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Buffer:
0.2 mg Na₂HPO₄, 0.9 mg NaCl, 5 mg BSA, 0.05 mg Thimerosal, 0.05 mg Sodium azide.
Immunogen:
A synthetic peptide corresponding to a sequence in the middle region of human EDA, identical to the related mouse and rat sequences.
Uniprot:
Q92838
Synonyme:
ECTD1;Ectodermal dysplasia protein;ectodysplasin-A;ED1;ED1-A1;ED1-A2;EDA-A1;EDA-A2;EDA1;EDA2;HED;HED1;ODT1;oligodontia 1;STHAGX1;TNLG7C;tumor necrosis factor ligand 7C;X-linked anhidroitic ectodermal dysplasia protein;XHED;XLHED
Weitere Details:
The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Versandbedingungen:
Blue Ice