PIPA597297

COX3 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA597297-Each-of-1 In Stock ₹ 46,502.50

PIPA597297 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

COX3

Classification

Polyclonal

Conjugate

Unconjugated

Gene

MT-CO3

Gene Alias

ACI60_gp01, Co3, Coiii, COX3, COXIII, cytchrome c oxidase sububnit 3, Cytochrome c oxidase polypeptide III, Cytochrome c oxidase subunit 3, cytochrome c oxidase subunit III, mitochondrially encoded cytochrome c oxidase III, Mtco3, mt-Co3, OXI2, Q0275

Host Species

Rabbit

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

17710, 26204

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Western Blot

Concentration

0.36 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide, pH 7.3

Gene Accession No.

P00416, P05505

Gene Symbols

MT-CO3

Immunogen

A synthetic peptide corresponding to a sequence within amino acids 1-100 of mouse MT-CO3 (NP_9043341)

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Mouse, Rat

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PIPA5103402

--

Img

Novus Biologicals

NB273648

--

Img

Thermo Scientific

PIPA5106809

--

Img

Thermo Scientific

PIPA5106811

--

Img

Thermo Scientific

PIPA596391

--

Img

Novus Biologicals

N270427J646

--

Img

Novus Biologicals

NB489214

--

Img

Novus Biologicals

NB489205

--

Description

  • Immunogen sequence: MTHQTHAYHM VNPSPWPLTG AFSALLLTSG LVMWFHYNSI TLLTLGLLTN ILTMYQWWRD VIREGTYQGH HTPIVQKGLR YGMILFIVSE VFFFAGFFWA; Positive Samples: Mouse liver, Rat liver; Cellular Location: Mitochondrion inner membrane, Multi-pass membrane protein COX3 is a multi-pass membrane protein
  • It belongs to the cytochrome c oxidase subunit 3 family
  • Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency)
  • Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.