PIMA515771

HAX1 Monoclonal Antibody (9G6C6), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA515771-Each-of-1 In Stock ₹ 47,481.50

PIMA515771 - 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

HAX1

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

PBS with 0.02% sodium azide

Gene Accession No.

O00165, Q7TSE9

Gene Symbols

Hax1

Immunogen

A 15 amino acid peptide near the amino terminus of human Hax1a.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human, Rat

Product Type

Antibody

Isotype

IgG3

Applications

Western Blot

Clone

9G6C6

Conjugate

Unconjugated

Gene

Hax1

Gene Alias

FLJ17042; FLJ18492; FLJ93803; Hax1; HAX-1; HCLS1 (and PKD2) associated protein; HCLS1 associated protein X-1; HCLS1 associated X-1; HCLS1-associated protein X-1; HCLSBP1; HS1 binding protein; HS1-associated protein X-1; HS1-associating protein X-1; HS1-binding protein 1; HS1BP1; HSP1BP-1; mHAX-1s; OTTHUMP00000034190; RP11-137P24.1; SCN3; SIG-111; Silg111

Host Species

Mouse

Purification Method

Protein A

Regulatory Status

RUO

Gene ID (Entrez)

10456, 291202

Content And Storage

-20°C

Form

Liquid

Related Products

Img

Thermo Scientific

PIMA515770

--

Img

Thermo Scientific

PIMA515769

--

Img

Thermo Scientific

PIMA514974

--

Img

Thermo Scientific

PIMA515552

--

Img

Thermo Scientific

PIMA515767

--

Img

Thermo Scientific

PIMA515768

--

Img

Thermo Scientific

PIMA515470

--

Img

Thermo Scientific

PIMA515780

--

Description

  • The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases
  • It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin
  • It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body
  • Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease
  • Two transcript variants encoding different isoforms have been found for this gene.