MABS1161MI

MilliporeSigma™ PYCR1, Mouse, Unlabeled, Clone: 2D9.1,

Manufacturer: MilliporeSigma™

Select a Size

Pack Size SKU Availability Price
Each of 1 MABS1161MI-Each-of-1 In Stock ₹ 40,292.08

MABS1161MI - Each of 1

₹ 40,292.08

In Stock

Quantity

1

Base Price: ₹ 40,292.08

GST (18%): ₹ 7,252.574

Total Price: ₹ 47,544.654

Antigen

PYCR1

Classification

Monoclonal

Concentration

Please refer to lot specific datasheet.

Formulation

Purified mouse monoclonal IgG2bκ antibody in buffer containing 0.1M Tris-Glycine (pH 7.4), 150mM NaCl with 0.05% Sodium Azide.

Gene Accession No.

P32322

Immunogen

GST-tagged recombinant protein corresponding to the C-terminal of human PYCR1.

Quantity

100 μg

Research Discipline

Signaling

Gene ID (Entrez)

NP_001269209

Target Species

Human

Form

Purified

Applications

Western Blot

Clone

2D9.1

Conjugate

Unconjugated

Gene

PYCR1

Host Species

Mouse

Purification Method

Protein G Purified

Regulatory Status

RUO

Primary or Secondary

Primary

Test Specificity

Expected to react with spliced isoforms 1 and 3, but not isoform 2, reported by UniProt P32322).

Content And Storage

Stable for 1 year at 2°-8°C from date of receipt.

Isotype

IgG2b κ

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Description

  • Pyrroline-5-carboxylate reductase 1, mitochondrial (EC 1.5.1.2; UniProt P32322; also known as P5C reductase 1, P5CR 1) is encoded by the PYCR1 (also known as ARCL2B, ARCL3B) gene (Gene ID 5831) in human
  • Pyrroline-5-carboxylate (P5C) reductase (PYCR1) is a mitochondrial enzyme that utilizes NAD(P)H as cofactor and catalyzes the convertion of P5C to L-proline, as well as the coversion of δ1-piperideine-6-carboxylate (P6C) to L-pipecolic acid, both of which are intermediates in the catabolism pathway of the essential amino acid L-lysine
  • PYCR1 gene mutations are associated with the autosomal recessive disorder cutis laxa type II, menifested with premature aging features such as joint laxity and wrinkled/lax skin, as well as developmental delay.