PIPA5143150

Aldolase A Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5143150-Each-of-1 In Stock ₹ 40,317.00

PIPA5143150 - Each of 1

₹ 40,317.00

In Stock

Quantity

1

Base Price: ₹ 40,317.00

GST (18%): ₹ 7,257.06

Total Price: ₹ 47,574.06

Antigen

Aldolase A

Classification

Polyclonal

Conjugate

Unconjugated

Gene

ALDOA

Gene Alias

ALDA; Aldo1; Aldo-1; ALDOA; Aldolase 1; aldolase 1, A isoform; aldolase A; aldolase A, fructose-bisphosphate; aldolase, fructose-bisphosphate A; epididymis secretory sperm binding protein Li 87p; fructose-1,6-bisphosphate triosephosphate-lyase; fructose-bisphosphate aldolase A; GSD12; HEL-S-87p; Lung cancer antigen NY-LU-1; muscle-type aldolase; RNALDOG5; unnamed protein product

Host Species

Goat

Purification Method

Ammonium sulfate precipitation

Regulatory Status

RUO

Gene ID (Entrez)

11674, 226, 24189

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Isotype

IgG

Applications

Western Blot

Concentration

0.5 mg/mL

Formulation

TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3

Gene Accession No.

P04075, P05064, P05065

Gene Symbols

ALDOA

Immunogen

Peptide with sequence C-QKADDGRPFPQ.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Form

Liquid

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Description

  • Additional Information: This antibody is expected to recognize both reported isoforms (P_000025.1; NP_001230106.1)
  • This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:128,000
  • Aldolase encodes a member of the class I fructose-bisphosphate aldolase protein family
  • The encoded protein is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate
  • Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development
  • Mutations in this gene have been associated with Glycogen Storage Disease XII, an autosomal recessive disorder associated with hemolytic anemia
  • Disruption of this gene also plays a role in the progression of multiple types of cancers
  • Related pseudogenes have been identified on chromosomes 3 and 10.