50-172-6185

CCM3/PDCD10 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech

Manufacturer: Proteintech Group Inc

Select a Size

Pack Size SKU Availability Price
Each of 1 50-172-6185-Each-of-1 In Stock ₹ 44,150.23

50-172-6185 - Each of 1

₹ 44,150.23

In Stock

Quantity

1

Base Price: ₹ 44,150.23

GST (18%): ₹ 7,947.041

Total Price: ₹ 52,097.271

Antigen

CCM3/PDCD10

Classification

Polyclonal

Conjugate

Unconjugated

Gene

PDCD10

Gene Alias

CCM3, PDCD10, programmed cell death 10, TFAR15

Host Species

Rabbit

Purification Method

Antigen Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

11235, 494345, 56426

Content And Storage

-20°C

Form

Liquid

Applications

Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot

Concentration

0.32 mg/mL

Formulation

PBS with 50% glycerol and 0.1% sodium azide; pH 7.3

Gene Accession No.

Q6NX65, Q8VE70, Q9BUL8

Gene Symbols

Pdcd10

Immunogen

CCM3/PDCD10 Fusion Protein Ag0348

Quantity

150 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

Related Products

Img

Proteintech Group Inc

50-100-2979

--

Img

Proteintech Group Inc

50-172-6251

--

Img

Proteintech Group Inc

50-172-6268

--

Img

Proteintech Group Inc

50-172-6227

--

Img

Proteintech Group Inc

50-172-6123

--

Img

Proteintech Group Inc

50-172-6171

--

Img

Proteintech Group Inc

50-172-6225

--

Img

Proteintech Group Inc

50-172-6067

--

Description

  • 10294-2-AP is a rabbit polyclonal antibody raised against the full-length PDCD10 of human origin
  • This gene encodes an evolutionarily conserved protein associated with cell apoptosis
  • The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway
  • It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent
  • Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages
  • Multiple alternatively spliced variants, encoding the same protein, have been identified.