GTX66497
ELMOD3 antibody
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX66497
- Zusätzliche Namen:
- ELMO domain containing 3 , DFNB88 , LST3 , RBED1 , RBM29
- Anwendung:
- WB
- 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:
- PBS, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- Recombinant funsion protein containing a sequence corresponding to amino acids 290-381 of human ELMOD3 (NP_001128493.1).
- Uniprot:
- Q96FG2
- Synonyme:
- deafness, autosomal recessive 88;DFNA81;DFNB88;ELMO domain-containing protein 3;ELMO/CED-12 domain containing 3;liver-specific organic anion transporter 3TM12;LST3;organic anion transporter LST-3b;RBED1;RBM29;RNA binding motif and ELMO/CED-12 domain 1;RNA-binding motif and ELMO domain-containing protein 1;RNA-binding motif protein 29;RNA-binding protein 29
- Weitere Details:
- This gene encodes a member of the engulfment and cell motility family of GTPase-activating proteins that regulate Arf GTPase proteins. Members of this family are defined by a conserved engulfment and cell motility domain. In rat cochlea, the encoded protein is found in stereocilia, kinocilia and cuticular plate of developing hair cells suggesting a function for this protein in cochlear sensory cells. An allelic variant of this family has been associated with autosomal recessive nonsyndromic deafness-88 in humans. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]
- Versandbedingungen:
- Blue Ice