PIPA532157

GBAS Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA532157-Each-of-1 In Stock ₹ 46,502.50

PIPA532157 - 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

GBAS

Classification

Polyclonal

Conjugate

Unconjugated

Gene

NIPSNAP2

Gene Alias

4-nitrophenylphosphatase domain and non-neuronal SNAP25-like 2; AV006093; GBAS; glioblastoma amplified sequence; glioblastoma-amplified sequence; nipsnap homolog 2; NIPSNAP2; Protein NipSnap homolog 2

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

14467, 2631

Content And Storage

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

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

PBS with 1% BSA, 20% glycerol and 0.01% thimerosal; pH 7

Gene Accession No.

O55126, O75323

Gene Symbols

NIPSNAP2

Immunogen

Recombinant fragment corresponding to a region within amino acids 1 and 225 of Human GBAS

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

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Description

  • Recommended positive controls: A549, H1299, HCT116
  • Predicted reactivity: Mouse (93%), Rat (95%), Zebrafish (84%), Chicken (90%), Bovine (94%)
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • GBAS encodes a protein belonging to the NipSnap family, which is believed to participate in vesicular transport
  • This protein is primarily found in mitochondria and is involved in oxidative phosphorylation
  • A non-functional version of this gene is located on the long arm of chromosome 2
  • Multiple isoforms of this gene have been identified due to alternative splicing
  • NIPSNAP2 is linked to several diseases such as Phosphoserine Phosphatase Deficiency and Mast Syndrome.