PIMA515854

OTX2 Monoclonal Antibody (1H12C4B5), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA515854-Each-of-1 In Stock ₹ 57,583.00

PIMA515854 - Each of 1

₹ 57,583.00

In Stock

Quantity

1

Base Price: ₹ 57,583.00

GST (18%): ₹ 10,364.94

Total Price: ₹ 67,947.94

Antigen

OTX2

Classification

Monoclonal

Concentration

Conc. Not Determined

Formulation

ascites with 0.03% sodium azide

Gene Accession No.

P32243, P80206, Q64201

Gene Symbols

OTX2

Immunogen

Purified recombinant fragment of human OTX2 expressed in E. Coli.

Regulatory Status

RUO

Gene ID (Entrez)

18424, 305858, 5015

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

ELISA, Flow Cytometry, Immunocytochemistry, Immunohistochemistry, Western Blot

Clone

1H12C4B5

Conjugate

Unconjugated

Gene

OTX2

Gene Alias

CPHD6; E130306E05Rik; homeobox Otx2; homeobox protein OTX2; MCOPS5; orthodenticle homeobox 2; orthodenticle homolog 2; OTX; OTX2

Host Species

Mouse

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG1

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Description

  • MA5-15854 targets OTX2 in indirect ELISA, FACS, IF, IHC, and WB applications and shows reactivity with Human samples
  • The MA5-15854 immunogen is purified recombinant fragment of human OTX2 expressed in E
  • Coli
  • MA5-15854 detects OTX2 which has a predicted molecular weight of approximately 32kDa
  • OTX2 is a 289 amino acid containing protein encoding a member of the bicoid sub-family of homeodomain-containing transcription factors
  • It has two known alternative splice variants with distinct isoforms though presence of other isoforms cannot be excluded
  • The protein is an early marker of endodermal differentiation of embryonic stem cells and may play a role in the development of the brain and the sensory organs
  • The protein may bind to BCD target sequence (BTS): 5-'TCTAATCCC-3'
  • Defects in OTX2 are the cause of microphthalmia syndromic type 5 (MCOPS5).