PIMA532869

KIDINS220 Monoclonal Antibody (3-B6), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA532869-Each-of-1 In Stock ₹ 47,481.50

PIMA532869 - Each of 1

₹ 47,481.50

In Stock

Quantity

1

Base Price: ₹ 47,481.50

GST (18%): ₹ 8,546.67

Total Price: ₹ 56,028.17

Antigen

KIDINS220

Classification

Monoclonal

Concentration

2 mg/mL

Formulation

PBS with 0.2% BSA, 40% Glycerol and 0.05% sodium azide, pH 7.4

Gene Accession No.

Q9ULH0

Gene Symbols

Kidins220

Immunogen

Recombinant protein with Human kinase D-interacting substrate 220 aa 1601-1771

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG1

Applications

Immunocytochemistry, Immunohistochemistry, Western Blot, Western Blot

Clone

3-B6

Conjugate

Unconjugated

Gene

Kidins220

Gene Alias

3110039L19Rik, AI194387, AI316525, ankyrin repeat-rich membrane spanning, ankyrin repeat-rich membrane spanning protein, ankyrin repeat-rich membrane-spanning protein, ARMS, C330002I19Rik, KIAA1250, KIDINS220, kinase D-interacting substance 220, kinase D-interacting substance of 220 kDa, kinase D-interacting substrate 220, kinase D-interacting substrate 220kDa, kinase D-interacting substrate of 220 kDa, kinase D-interacting substrate, 220kDa, MGC163482, mKIAA1250, truncated KIDINS220

Host Species

Mouse

Purification Method

Protein A

Regulatory Status

RUO

Gene ID (Entrez)

57498, 77480

Content And Storage

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

Form

Liquid

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Description

  • Mouse Monoclonal Antibody This gene encodes a transmembrane protein that is preferentially expressed in the nervous system where it controls neuronal cell survival, differentiation into exons and dendrites, and synaptic plasticity
  • The encoded protein interacts with membrane receptors, cytosolic signaling components, and cytoskeletal proteins, serving as a scaffold that mediates crosstalk between the neurotrophin pathway and several other intracellular signaling pathways
  • Aberrant expression of this gene is associated with the onset of various neuropsychiatric disorders and neurodegenerative diseases, including Alzheimer's disease
  • Naturally occurring mutations in this gene are associated with a syndrome characterized by spastic paraplegia, intellectual disability, nystagmus and obesity
  • Alternative splicing results in multiple transcript variants.