PIPA5143263

HMBS Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5143263-Each-of-1 In Stock ₹ 40,317.00

PIPA5143263 - 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

HMBS

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Hmbs

Gene Alias

alternative name: porphobilinogen deaminase; HEM3; hemC; HMBS; Hydroxymethylbilane synthase; PBG D; PBGD; PBG-D; PORC; Porphobilinogen deaminase; porphyria, acute; Chester type; pre-uroporphyrinogen synthase; similar to Porphobilinogen deaminase (Hydroxymethylbilane synthase) (HMBS) (Pre-uroporphyrinogen synthase) (PBG-D); T25658; Ups; uroporphyrinogen I synthase; uroporphyrinogen I synthetase; URO-S; Uros1

Host Species

Goat

Purification Method

Ammonium sulfate precipitation

Regulatory Status

RUO

Gene ID (Entrez)

3145

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Isotype

IgG

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

0.5 mg/mL

Formulation

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

Gene Accession No.

P08397

Gene Symbols

Hmbs

Immunogen

Peptide with sequence C-HLEFRSIRGNLNTR.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human

Form

Liquid

Related Products

Img

Thermo Scientific

PIPA5143283

--

Img

Thermo Scientific

PIPA5143152

--

Img

Thermo Scientific

PIPA5142734

--

Img

Thermo Scientific

PIPA5143304

--

Img

Thermo Scientific

PIPA5143024

--

Img

Thermo Scientific

PIPA5143139

--

Img

Thermo Scientific

PIPA5142739

--

Img

Thermo Scientific

PIPA5143140

--

Description

  • Additional Information: This antibody is expected to recognize all reported isoforms (NP_000181.2; NP_001019553.1; NP_001245137.1; NP_001245138.1)
  • This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:32,000
  • PBGD (porphobilinogen deaminase), also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway
  • PBGD belongs to the HMBS (hydroxymethylbilane synthase) family
  • Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP)
  • AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.