Skip to content

View Spec Sheet

open_in_new
  1. Shop all
  2. Polyclonal

GTX88043

NDUFS6 antibody, Internal

Cannot supply to this region.

SKU:
GTX88043
Additional Names:
NADH:ubiquinone oxidoreductase subunit S6 , CI-13kA , CI-13kD-A , CI13KDA , MC1DN9
Application:
WB, IHC-P
Concentration:
0.50 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Ammonium Sulfate Precipitated; Affinity Purified
Storage Conditions:
-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.
Supplier:
Genetex
Host:
Goat
Reactivities:
Human, Mouse, Rat
Buffer:
TBS, 0.5% BSA, 0.02% Sodium azide.
Immunogen:
Peptide with sequence C-RIRFVGRQKEVNEN, from the internal region of the protein sequence according to NP_004544.1.
Uniprot:
O75380
Synonyms:
CI-13kA;CI-13kD-A;CI13KDA;complex I 13kDa subunit A;Complex I-13kD-A;complex I, mitochondrial respiratory chain, 13-kD subunit;MC1DN9;NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase);NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial;NADH-ubiquinone oxidoreductase 13 kDa-A subunit;NADH:ubiquinone oxidoreductase NDUFS6 subunit
Extra Details:
This gene encodes a subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.[provided by RefSeq, Oct 2009]
Shipping Conditions:
Blue Ice